Complete The Cytology of Soft Tissue Tumours Monographs in Clinical Cytology 1st Edition M. Akerman PDF For All Chapters
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The Cytology of Soft Tissue Tumours Monographs in
Clinical Cytology 1st Edition M. Akerman Digital Instant
Download
Author(s): M. Akerman, Henryk A. Domanski,
ISBN(s): 3805575947
Edition: 1
File Details: PDF, 8.75 MB
Year: 2003
Language: english
nog!!phs In <II til C)'lOI09LY _ _
Ed.lor: SJt Of II
Vol. 16
-fins kerman
Henryk A. Domansk"
o f
o
· .
The Cytology of Soft Tissue Tumours
Monographs in
Clinical Cytology
Vol.16
Series Edjtor
KARGER
The Cytology of
Soft Tissue Tumours
Including contribution by
Akerman. Mdns.
The cytology of soft tissue tumours I MAns Akennan, Henryk A. Domanski; in
collaboration with Andcrs Rydholm, Brigina Carlen.
p.; cm. - (Monogrnphs in clinical cytology; vol. 16)
Includes bibliographical references and index.
ISDN 3-8055-7594-7
I. Solllissue tumors-Cytodiagnosis. 1. Domanski. Henryk A. II. Title. Ill. Series.
[DNLM: I. Cytological Techniques. 2. Soft Tissue Neoplasms. WD 375 A314c 2003]
RC280.S66A3472oo3
616.99'207582-dc21 2003054510
Bibli"l!rnphic Indkes. This publication i. liSle<! ill bib/i_ All rights resem:d. No pon ofthi. publicalion may be
"l!J'IIlhi<; "",,·icc•. incillding eum:llt COIItrols- and Index translated inlo other Jan¥uages. reproduced 01" ulilil.ed in
Me<!icus. any form 01" by any mc'fI'j .kctnmic 01" mechanic.l. ;nclud-
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employed drull.
Contents
IX Preface
X Acknowledgements
Chapter 1
, Soft Tissue Tumours - Basic Information
Chapter 2
2 Fine Needle Aspiration of Soft Tissue Tumours
2 Surgical Biopsy, Core Needle Biopsy or Fine Needle Aspiration in the Primary Diagnosis
3 Diagnostic Accuracy of Fine Needle Aspimlion Biopsy
4 Pitfalls in the Fine Needle Aspiration of Soft Tissue Tumours
4 Complications of Fine Needle Aspiration of Soft Tissue Tumours
4 Fine Needle Aspiration Cytology Procedure
5 Classification of the Cytodiagnosis
6 The Final Evaluation of a Soft Tissue TurnOUT Aspirate
6 Ancillary Diagnostic Methods Supplementing the Cytodiagnosis
Chapt... 3
Chapter -4
Chapter 5
Chapter 6
103 Cytological Classification of Soft Tissue Tumours Based on the Principal Pattern
103 Pleomorphic Pattern
103 pindle ell Pattern
103 Myxoid Patt rn
103 mall Round/Ovoid ell Pattern
107 Epithelioid Cell Pattern
109 References
113 Index
VI Contents
Preface
The cytological diagnosis of soft tissue tumours, ba ed core needle biopsy offer a number of advantages when used
on fine needle a pirate , ha been debated and at times dis- in the primary diagnosis of soft tis ue tumour .
couraged except in the diagnosi of lipoma. Soft ti ue The purpo e of thi book i to facilitate the cytological
tumours are relatively rare in spite of the fact that more than evaluation ofF A smear from soft ti sue tumours and ug-
100 benign ubtypes, over 50 variant of arcoma and a gest cytological criteria for a histotype diagnosis. The aim is
number of 'border-line' entities have been described. foremost to describe and illustrate the most common entities
lndi idual cytopathologi tare thu not likely to encounter and tho e rare tumour where cytological feature have been
many of the less common variants of oft tissue tumours described in case-reports and in small series.
during their training and may only occasionally needle them The diagnostic u e of ancillary methods is also discus ed
in their later practice. It ha been trongly recommended and illu trated.
that the primary morphological diagnosis of malignant soft The selection of entities which will be presented, their
tis ue tumours as well as other investigations and treatment diagno tic features and differential diagno tic considerations
hould be performed at multidisciplinary centre. Tn prac- are mainly based on the experience with F in the primary
tice, however, it is not possible to refer all patient with soft diagnosis of soft tissue tumours in patients referred to the
tis ue tumour to a musculo keletal tumour centre for pri- Musculoskeletal Tumour Centre, University Hospital, Lund,
mary work-up. Tumours are usually considered to be u pi- Sweden over a 25-year period. Case from the oft tissue
cious if they are large (>5 cm) or deep-seated (inter-or tumour registry of the Scandinavian Sarcoma Group (a mul-
intramuscular). Till implies that the management of the tidisciplinary association with members from all Nordic
majority of oft ti ue tumour i undertaken in general ho - countrie ) have al 0 been u ed. The illu tration have been
pitals. culled from cases in the file of the Department of Pathology
The use of pedal diagnostic methods has led to greater and Cytology Lund University Hospital, which now contains
accuracy in histopathological diagno i in this tumour group. smears from more than 3,000 soft tissue tumours needled
The u e of ancillary method is al 0, no doubt, nece sary in between 1972 and 2002.
many ca e when fine needle a piration ) and cytodi-
agno i i used in primary diagno i making surgical biopsy
unnece sary. A ha repeatedly been demonstrated in other Mans Akerman
tumour entitie , the u e of F A instead of urgical biop y or HelUykA. Domanski
Preface IX
Acknowledgements
The authors thank Dr. vante Orell, Clinpath Laboratories I would like to thank Drs. Annika Dejmek and Karin
Adelaide, Australia for hi help. Svante Grell i the cientific Lindholm of the Department of Clinical Pathology and
editor for the erie Monograph in CLinical Cytology and hi Cytology ofth Uni er ity Ho pital MA of Malmo, weden,
comments and revision of the text have been invaluable. We for introducing me to the fantastic world of cytology and
thank Dr. Walter Ryd, Division of Cytology, Department Dr. Man Akerman of th Department of Pathology and
of Pathology ahlgren's Hospital, Gothenburg, weden for Cytology, University Hospital Lund, weden, my teacher and
letting u use illustrations of hi ca e of desmoplastic small friend, for sharing his broad experience in aspiration cytology.
round cell tumour and Dr. L nnart Mellblom, D partment of
Pathology and Cytology, Kalmar Hospital, Kalmar, Sweden Henryk A. Domanski
for contributing information regarding hi ca e of 0 sifying
fibromyxoid tumour. We also thank Prof. Frederik Mertens
Department of Clinical Genetic , Univer ity Hospital Lund,
for providing figure 6 and 7.
Man Akerman
HenrykA. Domanski
x Acknowledgement
Chapter 1
The incidence of soft tissue tumours is difficult to estimate, Ewing's sarcoma (ES)/primitive neuroectodermal tumour
especially the ratio of benign to malignant. Benign Ie ion are (P ET) family of tumour, rhabdomyo arcoma and pleo-
u ually estimated to be approximately 100 times more fre- morphic liposarcoma are all high-grade malignant, while
quent than sarcomas. Sarcomas are relatively rare, constituting well-differentiated liposarcoma, paucicellular myxoid
about I% of all malignant tumours. In Sweden, the annual liposarcoma, infantile fibrosarcoma and dermatofibro-
incidence of sarcomas of the locomotor system ha been esti- sarcoma protuberans are low grade. Provided that a A
mated to be 1.4/100000. Age-specific incidence rates clearly mear from a sarcoma i technically satisfactory and moder-
demonstrate that soft ti sue sarcoma of the locomotor sy tern ately cellular it i po sible to grade most sarcomas into low-
b com mor common with increa ing age; in on study their grade or high-grade cat gories.
incidence wa 8.0/100,000 for patient 80 year or older. The diagno tic workup of a oft ti ue tumour before ur-
Generally oft ti ue arcoma is more common in males gery include site, type diagnosis and location in relation to
but gender as well as age-related incidence depends on the the surrounding tissues, especially major nerves and ves els.
hi togenetic type. Magnetic re onance imaging i usually be t for thi evalua-
oft ti ue tumour are u ually cia ified hi tog n tically tion. For patient with arcoma lung radiograph and ome-
and within each group they are divided into benign Ie ion time computed tomography scan are obtained; it is
sarcomas and intermediate or borderlin tumours. impOltant to determine whether metastatic disease is present
In this atlas we u e the classification proposed by in order to plan management.
Kemp on et al. [I] and Weis and Goldblum [2], re pectively. In an attempt to predict outcome, to determine appropriate
Since knowledge of the hi totype of a sarcoma alone i not treatment and to make compari on between the results of dif-
alway ufficient to predict clinical cour e and choice ofther- ferent centre everal taging y tern have been proposed.
apy a number of grading systems, based on a variety of However, there is no general consen u a to which one to use.
parameters have been uggested and debated. The most fre- Two which are commonly used are the American AJCC/UICC
quent parameter u ed are cellularity, differentiation, cellular system (American Joint Committee/International Union
and nuclear pleomorphism mitotic rate, necrosis and vascu- Against Cancer) which is based on depth, grade and size, and
lar invasion. The number of grades varies; two, three and four the French F CLCC system (French Federation of Cancer
grade hav been propo d. How ver the hi totype in its If enter) ba d on the arne factors but with a more detailed
may indicate tumour grad . For example, the extraskeletal definition of malignancy grade.
Surgical Biopsy, Core Needle Biopsy or Fine needling of oft tissue masses in children in whom a brief gen-
Needle Aspiration in the Primary Diagnosis ral ana thesia may be needed. An evaluation of the a pirate
within 10-15 min after needling i po ible with a rapid haema-
[n the majority of mu culo keletal tumour centres the toxylin-eosin (HE) or Diff-Quik tain. The adequacy of the
definitive diagnosis of soft ti ue tumours, especially u- material can thus be checked while the patient is waiting, and a
p ct d arcoma , is bas d on the histopathological evaluation prelinlinary diagnosi i sometimes po ible. The purpo e of a
of a biop y ample or a core needle biop y with an outer prelinlinary evaluation is 2-fold: it might give important infor-
diam ter of 1.2-1.4 mm. mation on the type of ancillary diagno tic that hould be u ed
Although A with needles having an outer diameter of and the urgeon can inform the patient and sugge t further
0.4-0.8 rom has been a uIDver ally accepted diagno tic investigations or treatment at hislher flrst visit. Since the diag-
method in the definitive diagnosis of various tumour entitie nosis and treatment of soft tis ue sarcoma should preferably be
for many year, objection have been rai ed to FNA in the centralized to multidi ciplinary tumour centres, it i important
primary diagno i of oft ti sue tumours. The main objection as regard referred pati nts that the nece sary information i
has been the postulated inability to a pirate tumour material obtained rapidly and the number of visits are a few a po si-
ufficient for reliable histotype diagnosis with a thin needle. ble. Experience from the Musculo keletal Tumour Centre at the
Due to the numerou subtypes and morphological hetero- niversity Hospital of Lund has hOWD that for patients
geneity among pecific entitie, oft ti u tumour have referred to th centr for tumours suspicious ofmalignancy one
been con idered to pose some ofthe greatest diagnostic chal- vi it was usually ufficient when the tumour proved to be
lenges in surgical pathology and routine light microscopy is benign at the combined evaluation of clinical examination,
often not ufficient for a diagno tic evaluation. Additional fNA diagno i and radiographic examination, if any [3].
diagnostic methods such as histochemistry, immunohisto- ore needle biop y i a1 0 an outpatient procedure, but
chemistry, electron micro copy (EM), D A ploidy analysi a preliminary diagnosis is less feasible than with FNA. F A
and chromo omal analy i and molecular genetic often have also permits sampling of different part of large tumour to
to be applied to reach a reliable diagno is. e aluate tumour heterogeneity, pro iding important informa-
However, article and book chapters on oft tissue tion in, for example, lipomatou tumour.
tumours as a target for FNA began to appear at the beginning A novel diagnostic approach recently tested at our centre is
of the 1980 . The first ca eerie pu bli hed were often mall a combination of fNA and core needle biopsy in selected
and the diagno tic workup was not critically inve tigated. patient referred for FNA. The FNA as well a the core needle
In spite of a negative attitude to FNA among surgeons, biopsy is perform d by the cytologist at the same visit. This
oncologists and pathologists, it has been shown that the same approach combines the advantages of both sampling methods:
advantage which have made F A a fir t-choice diagno tic ampling from different parts of large tumours, a rapid prelim-
approach in breast tumour, thyroid tumour, alivary gland inary report, the po ibility to evaluate the ti sue architecture in
tumour or malignant lymphomas are al 0 applicabl in the the core biop y (often difficult in an F mear) (fig. I a, b).
diagnostic workup of a oft ti sue tumour. In addition material sufficient for various ancillary methods
FNA of a suspected soft tissue tumour is an outpatient pro- such as irnmunohi tochemistry, EM and cytogenetic/molecular
cedure. 0 ane the ia i neces ary. One exception is the genetic analyses [4] i obtained with greater certainty.
Diagnostic Accuracy of Fine Needle Aspiration but the case eries have been mall and the number of
Biopsy arcomas evaluated often few [5-8]. Only a few large erie
from multidi plinary centres have been publi hed. In a
Several reports of diagnostic accuracy (i.e. differentiation retrospective 20-year study of 517 tumour , 315 benign and
of benign vs. malignant proce s) have been publi hed. 202 arcoma cases of the extremities and trunk from the
Accuracy has been greater than 90% in most publications Mu culoskeletal Tumour Centre, Univer ity Ho pital of
Pitfalls in the Fine Needle Aspiration of Soft Complications of Fine Needle Aspiration of
Tissue Tumours Soft Tissue Tumours
There are three important limitations to F A in the In our experience of F of more than 25 year in the
diagnosis of oft ti sue tumours [11-12]. primary diagnosis of soft tis ue tumours in patients referred
(I) The needle may miss the tumour and a false diagnosis to our Mu culo keletal TWTIour Centre we have ne er expe-
i made on the basi of cell aspirated from the tis ue rienced any severe complication. Patients have, at mo t,
urrounding it. Reactive cellular change in the adipo e tis- complained of tendem s and, in ca es of ubcutaneous
sue may mimick lipo arcoma and p eudomalignant reactive tumours, of haemorrhage. We have not seen a single case of
changes in fibroblasts and myofibroblasts may suggest infection and never experienced clinical signs of sarcoma
a pleomorphic arcoma. Thi diagnostic difficulty most often cell eeding in the needle track. It i to be remembered that
occur when mall, deep-seated, inter- or intramu cular F A i the lea t ti ue-de tructi e in asive diagno tic
tumour are needled. It is important that the per on perform- method.
ing the aspiration has enough experience to be able to evalu-
ate whether the material obtained might be consi tent with
th tumour in que hon (ag , history, site, ize, and palpatory Fine Needle Aspiration Cytology Procedure
findings). It i recommended that mall, deep- eated twnours
be needled with ultra ound guidance. Practical Considerations
(2) Insufficient or technically suboptimal material may The aspiration technique is the arne a for other target
result in a false diagnosis or preclude any diagnosis at all. for FNA. We have found that a syringe holder which allows
The temptation of making a diagnosis on quantitatively or aspiration with one hand is es ential for succe s. Needle
qualitatively insufficient material must be resisted. It is wider than 22 gauge (0.7 mm) are very rarely necessary. The
a fact that some tumours are difficult to diagno e by FNA. length of the needle depend on the ite of the tumour. For
Va cular tumour mo t often yield predominantly blood and deep-seated tumours, needle with a tylet are recom-
very few cells and in various tumours rich in dilated vessels mended. The stylet strengthens the needle and prevents cells
the aspirates may be very bloody but contain very few from surrounding ti sue from being included in the mear.
tumour cell . Another difficulty i to obtain a ufficient Thorough palpation and e: timation of ize, ite and con i -
number of cells from tumours with an abundant collagenous tency of the tumour is e entia!. Since the surgeon often may
or hyalinized background matrix. Extensive necrosi , cy tic want to determine the point of in ertion of the needle, close
degeneration or haemorrhage can also make diagnostic communication with the urgeon is mandatory. If the
a piration very difficult. In general, however, with adequate urgeon doe not indicate the insertion point, the twnour i
ampling, it i po sible to obtain ufficient material for needled through the vertex. In ca e of u peeted sarcoma the
diagnosis. insertion point can, at the request of the urgeon be tattoed
(3) Mi interpretation of the material is, however, the so that the needle track can be removed at urgery (fig. 2).
main cause of false diagnoses. There are a number of Our policy is to perform at most 5 F A pa se , all through
the arne in ertion point. Due to tumour ti ue heterogeneity, When the treatment include neoadjuvant therapy (radio-
e peciaJly in large tumours, it i important to ample ti ue therapy or chemotherapy followed by urgery the
from differ nt part of tbe tumour. iliagno i mu t equal that of a hi topathological e aluation
The microscopic evaluation hould be based on both wet- a regard illstotype and malignancy grade.
fixed [HE or Papanicolaou (pap)] and air-dried [May- At pre ent neoadju ant therapy i u ed for rhabdomyosar-
Griinwald-Giemsa ( GG) or Diff-Quik] smears. coma, neuroblastoma the extra keletal EwingfP ET family
The wet-fixed material i uperior for e aluation of nuclear of tumour and in om centre elected ca of oft ti ue
detail such a chromatin structure and nucleoli willie the arcoma .
MGG taining giv exceU nt information on cytopla mic On the oth r hand, in ca e of a b nign oft ti u tumour
detail and the background matrix. or reactive soft ti sue Ie ion the surgeon often want to know
the hi totype in order to inform the patient of the two treat-
Cytodiagnosis ment option : ob ervation/follow-up or local excision.
One common objection to F A in the primary diagnosi Ob ervation may be ugge ted in the pseudosarcomatou
of oft ti sue tumour is the uppo ed inability to correctly soft tissue lesions, especially nodular fasciitis and pseudo-
and reliably diagno e the numerou different histotypes in malignant myositi 0 ifican and in case of lipoma or
mear . However the nece ary diagno tic level for a soft neurilemoma and de moid fibromato i . A helling out of
ti ue tumour i determined by the primary treatment envi - the tumour is sufficient treatment for most benign soft tissue
aged in the individual case. First of all the surgeon mu t tumour except de moid fibromato i , willch require more
know whether the tumour in que tion i a true oft ti ue exten ive margin due to i infiltrative growth.
Ie ion/tumour or a oft ti ue meta ta i or a primary oft
tis ue lymphoma. In ca e of arcoma the tandard treatment
in the majority of ca e i primary radical surgery ometime Classification of the Cytodiagnosis
followed by radiotherapy. The type of surgical intervention
d pend mor on the ite ( ubcutan 01lS or d p) ize and tandardiz d reporting i an ad antag both to the urg on
the relation of the arcoma to ve el nerv bundle and and to the cytopathologi 1. At our Mu culo keletal Tumour
perio teum than on the hi totype. Thu a reliable diagno i of Centre w have for many year u ed four main diagno e :
arcoma i sufficient for the surgeon in tho e ca es where benign, sarcoma, other malignancy or inconclusive.
primary radical surgery i the propo ed treatment. lnconclu i e means either that tbe material i in ufficent for
a b
Antibody'
Mu c1e- pecific actin Leiomyosarcoma - 0-90%+
Rhabdomyosarcoma -90%+
mooth mu cle actin ( MA) Leiomyosarcoma -90%+
Desmin Leiomyosarcoma -70-75%+
Rhabdomyosarcoma -9 95%+
D R T -90%+
xtrarenal malignant rhabdoid tumour (some)
Caldesmon Leiomyosarcoma
Myoglobin Rhabdomyosarcoma -40%+
MyoDI Rhabdomyosarcoma >90%+
-100 protein MP T -40-50%+
Round cell liposarcoma -60-70%+
Clear cell sarcoma -80%+
EMC -20-40%+
Synovial sarcoma -30%+
neurilemoma, leiomyo arcoma, solitary fibrous tumour and All antibodi u d in soft ti sue tumour diagno i are
occasionally in the type diagnosis of ynovial sarcoma. 1 is an uitable for formalin-fixed and paraffin-embedded ti ue
important diagno tic a et in the pecific diagno i ofangio ar- and well suited for the small tis ue of successful cell block
coma and small round cell arcomas. preparations (fig. 3a-c) (table 2).
We have found Ie on ceU block preparations from aspi- The diagoo tic value of EM is still significant in spite
rates more reliable than on cytocentrifuge preparation . of the vast u of immunostaining. EM in the diagno tic
36
I-t1-----------1 DNA Index: 1.41
Area: 108.4 IL2
f --t
C Cells: 41
::> 2 3 4 5
0 Second peak
u 24
=ai
0
Mass: 0.0 pg.
DNA index: 0.00
Area: 0.0 1L2
•
12 Cells: 0
II 1.1
Field count: 75
Tolal cell count: 120
6 7 8 9 10 11/12
0 8 16 24 32 Cells displayed: 100
DNA mass picograms Cells oft scale: 0
..
11:
__ '.84
0 92
.
1.11
1.11
1.84
1.09
1.39
0
1.35
0
1.<19
0
0.00
0.07
0.00
5.21
0.83
76.67 92
, o.
13 14 15 16 \ 17 18
I
...2.22
3.66
_ _ 2.22
2.22
3.66
4.«
0.00
2.72
0.00
0.00
2.58
0.00
0.00
0.22
0.00
0.00
6.37
0.00
0.00
5.83
0.00
0
7
0
- .--,-- -- ,
17.61 2.72 2.58 0.22 6.37 5.83 7 19 20 21 22 x X
Fig. 5. Image cytometry of a high-grade malignant oft tis ue Fig. 6. FNA of a myxoid liposarcoma processed for karyotyping.
arcoma. Aneuploid cell population. The typical translocation t(12; 16) i marked.
F M as well a rCM can be performed on fine needle An unequivocal non-diploid cell population indicates
a pirate . One ad antage with r M i that previou Iy tained arcoma and furthermore a high-grade sarcoma [45] while
a pirate may be de tained, re tained with Feulgen and a diploid or tetraploid hi togram i of no diagno tic value.
analyz d. We ha found D A ploidy analysi of limit d A di advantage with FCM is that false diploid hi tograms
diagnostic value in the evaluation of a soft tissue tumour aspi- may occur [62, 63]. Through comparative FCM and ICM
rate in the differential diagnosis of benignity and malignancy. analy es on the same ti sue specimen it has become evident
that diploid or inconclusive FCM hi tograms in ti ue transcripta e-polymera e chain reaction (RT-PCR; when the
pecimen as well a in aspirate hould be upplemented gene involved in a diagno tic chromo omal aberration, mo t
with ICM to avoid fat ere: ult . often a translocation, are known) are easier to perform on
ytogenetic analysis has emerged as a promising diag- FNA, because the number of cell necessary for these analyses
no tic adjunct in soft tis ue tumour diagno i . Karyotyping, are far Ie than for conventional karyotyping, and dividing
fluore cent in situ hybridization (Fl H) and molecular cell are not n ce ary (fig. 7). The hith rto known diagno tic
genetic analysis can be performed on FNA from muscu- chromosomal aberrations are listed in table 3.
loskel tal tumours [64-68] (fig. 6). FISH or reverse
One reason for a false-positive diagnosis of sarcoma in a with elongated cytoplasmic processes. The nuclei are
soft tis ue tumour a pirate is the mi interpretation of benign, rounded, ovoid or fusiform with regular chromatin and small
reactive cellular changes in benign condition. nucleoli, if any. The cell are een either a di sociated or in
small clusters or runs of loosely attached cells. Stripped
nucl i are not uncommon (fig. ).
Fibrous Tissue Reactive fibroblasts/myofibroblasts show irrespective of
cause, a wide variation in ize and shape. The cells become poly-
ormal fibrobla t myofibrobla t appear in F A am- hedral or triangular, often with rather abundant cytoplasm. They
pies as spindle-shaped cells with slender cytoplasm, often may show angulated cytopla mic extension or cytoplasmic
proce ses. The nuclei vary in size and shape (rounded, ovoid, Adipose Tissue
spindle- haped) and nucleoli may be large and prominent.
Binucleated cell are not uncommon (fig. 9a, b). ormal adipose tis ue i een as mall fragment or clus-
Typical example of the pleomorphic appearance of reac- ters of large cells with abundant univacuolated cytoplasm
tive fibrobla ts/myofibroblasts are seen in the pseudomalig- and small, dark, regular nuclei. A discrete network of thin
nant, benign oft tis ue Ie ion, e pecially in nodular fasciiti capillarie is often ob erved. Di ociated adipocyte are
and proliferative myositis. uncommon.
size and shape. They are rounded, polyhedral, strap-shaped or uniform in size and often harbour a prominent nucleolus. The
tadpole-like. The cytoplasm is den ely eosinophilic in HE and nuclei are typically arranged in row, eccentrically located
dark blue in MGG. The multiple nuclei are moderately large, (fig. lla-c).
Table 4. A ulllluary of benign 'pseudomalignant changes' in aspirated material from fibrous and adipose tissue and striated muscle
Regenerating muscle fibres are mainly found within A A summary of the reactive cytological changes in fibrou
sample from tumour infiltrating striated mu cleo Typical tissue, adipose tissue and striated muscle is pr sented in
example are infantile fibromato is colli and desmoid fibro- table 4.
matosis.
Pleomorphic lipomas may have a myxoid stroma and collagen A variable number of large cells with hyperchromatic
bundles similar to those in spindle cell lipoma are often pres- nuclei and eosinophilic cytoplasm (HE) both in the back-
ent. Transitional forms between pleomorphic and spindle cell ground and in tissue fragments
lipoma are fairly commOll. The giant cells stain for C034. A variable number of 'floret cells'
Clusters or runs of spindle cells seen in transitional forms
Differential diagnosis
Cytological features of pleomorphic lipoma (fig. 170, b) Well-differentiated liposarcoma (atypical lipomatous
Fragments of mature fat tumour)
• • ••
• • • •
• •
• •
•
•
• •
•
- • •
•
.-
•
• •
•
•
•
- •
•
•
Fig. 16. pindle cell lipoma. a Scattered pindle cell and fTagment
f lIagen-hyaline fibre in a myxoid background with mall fatty
vacuole. MGG. High magnification. b niform population of spin-
die cells with bland nuclei. HE. High magnification. c The collagen-
C ...... ""-.....:3 :;...._....:z"-- -='--_....;..._ hyaline fibre are brightly eo inophilic with HE.lligh magnification.
Cytological features or chondroid lipoma ((Ig. 20a-d) Chondrocyte-like cells sometimes seen in the back-
Variable amount of myxo-chondroid background matrix ground matrix
Clusters or groups of mature large adipocytes mixed with Differential diagnosis
clusters or groups of uni- or rnultivacuolated lipoblast- Myxoid liposarcoma
like cells Extraskeletal myxoid chondrosarcoma
Lipoblast-like cells have irregular nuclei of varying sizes.
often lobulated or grooved
• b
,'---- d
Fig. 20. Chondroid lipoma. a Low power vicw of groups of vacuo- background. MGG. High magnificlltion. c Lipoblast-like cells.
lated cells with a partly myxoid. partly fatty background. MOG. Low MOO. High magnification. d Wet-fi....ed smear showing irregular
magnification. b A group of chondroblast-like cells in a myxohyaline nuclei with folded nuclear membranes. HE. High magnification.
Tissue Sarcoma Registry of the Scandinavian Sarcoma Three large groups of liposarcomas arc identified: well-
Group (a multidisciplinary group with members from all differentiated/dedifferentiated, myxoid/round cell, and
Nordic coulitries) liposarcoma was the third moSI common pleomorphic.
sarcoma.
The majority of liposarcomas arc deep-seated, intra- or Well-Differemiated alld Dediffiremiated LiposG/Y:oma
intermuscular, and the most common sites are the extremi- Well-differentiated liposarcoma occurs most commonly
ties, trunk and retroperitoneum. in late adult life (age 60-70). About 75% are intramuscular
Histopathology Comment
There is a predominance of mature fat cells combined The cytological diagnosis of dedifferentiated liposarcoma
with a variable amount of atypical cells with irregular hyper- is based on the presence of mature fat cells and a highly
chromatic nuclei and multi vacuolated lipoblasts. The atypical cellular population. As these tumours are often large
lipoblasts are usually infrequent. The atypical cells are either it is important to collect material from various areas. espe-
situated among the mature fat cells or in fibrotic strands or cially from sites which arc considered non-lipomatous by
trabeculae, and are also commonly seen in the perivaseular radiographic imaging.
tissue or within the vessel walls.
Myxoid/Round Cell Liposarcoma
About 500!o of liposarcomas are diagnosed as myxoidl
Cytologicol feawres ofwelkJifferenrioted liposarcoma (~g.llo-d) round cell liposarcoma. These two variants share the same
A predominance of mature fat cells arranged in clusters cytogenetic abnormality: t( 12; 16)(q 13;p II) with fusion of
or sheets the CHOP gene on chromosome 12 with the TlS gene on
Variable presence of fusiform. rounded or polygonal. large chromosome 16.
atypical cells with irregular hyperchromatic nuclei
Rare multivacuolated lipoblaslS MYXOid Liposarcoma
Variable presence of fragments of fibrous tissue with I-listopathology
atypical cells Myxoid liposarcomas are multilobulated tumours with an
Differential diagnosis abundant myxoid matrix. A plexiform capillary vessel oct-
Upoma work is a typical finding and cellularity is rather low. The
Fat necrosis with lipophages tumour cell population is composed ofboth spindle cells and
,-----:>.
Fig. 22. Wcll-difTCTCnlialcd liposarcoma (atypical lipomatous magnification. c Multivacuolatcd lipoblasls may be presenl but are
d
lumour). a Scallered large cells with hyperchromatic nuclei within a not necessary for the diagnosis. MGG. High magnification.
fragment of mature adipose tissue. HE. Low magnification. b The d Multinucleated noret cells may also be present in well-differentiated
atypical cells often have irregular, hyperchromatic nuclei. HE. High liposarcoma. HE. High magnification.
"
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• b
Fig. 21. Myxoid liposarcoma. a Low power view showing the typi-
cal appearance of myxoid liposarcoma. MGG. Low magnification.
b Another low power view stained with HE. Note that the myxoid
background is less evident. Low magnil1cation. c This high pQY.'er
viC\\' shows a capillary network. muhivacuolatcd lipoblasls and
rounded tumour cells embedded in myxoid matrix. MGG. High
magnification.
myxoid background. The vessel fragments in myxofibrosar- Myxoid matrix and capillary network less conspicuous
coma are found in the background matrix and are non- than in myxoid liposarcoma
branching coarse fragments. Rounded tumour cells with scanty cytoplasm and
rounded nuclei with irregular chromatin
Round cell Liposarcoma Atypical lipoblam
Histopathology Mitoses may be found
Pure round cell Iiposllrcoma or foci of round cell liposar- Differential diagnosis
coma in myxoid liposarcoma arc composed of sheets of Other types of round cell sarcoma infiltrating adipose
rounded cells with scanty cytoplasm and rounded, atypical tissue
nuclei oOen with nucleoli. The myxoid background is lcss evi· Soft tissue metastasis of renal carcinoma
dent or absent. Atypical lipoblasts are present among the
tumour cells but may be difficult to identify. Comment
True round cell liposarcomas are rare. Most are com-
posed of both typical myxoid liposarcoma tissue and highly
Cytological features of round cell liposarcoma (fig. 240, h} cellular areas as described above. [n histopathology the
Variable proportions of dispersed tumour cells and highly terms paucicellular and cellular myxoid liposarcoma,
cellular tumour fragments respectively, have been proposed instead of myxoid and
Stripped nuclei common round cells. The metastatic potential is increased if 25% or
Sir, the great conflict now raging in the Old World has presented a
phenomenon in military science unprecedented in the annals of
mankind, a phenomenon that has reversed all the traditions of the
past as it has disappointed all the expectations of the present. A great
and warlike people, renowned alike for their skill and valor, have
been swept away before the triumphant advance of an inferior foe,
like autumn stubble before a hurricane of fire. For aught I know the
next flash of electric fire that simmers along the ocean cable may tell
us that Paris, with every fibre quivering with the agony of impotent
despair, writhes beneath the conquering heel of her loathed invader.
Ere another moon shall wax and wane, the brightest star in the
galaxy of nations may fall from the zenith of her glory never to rise
again. Ere the modest violets of early spring shall ope their
beauteous eyes, the genius of civilization may chant the wailing
requiem of the proudest nationality the world has ever seen, as she
scatters her withered and tear-moistened lilies o’er the bloody tomb
of butchered France. But, sir, I wish to ask if you honestly and
candidly believe that the Dutch would have overrun the French in
that kind of style if General Sheridan had not gone over there, and
told King William and Von Moltke how he had managed to whip the
Piegan Indians.
And here, sir, recurring to this map, I find in the immediate
vicinity of the Piegans “vast herds of buffalo” and “immense fields of
rich wheat lands.” [Here the hammer fell.]
[Many cries: “Go on!” “go on!”]
The Speaker—Is there any objection to the gentleman from
Kentucky continuing his remarks? The chair hears none. The
gentleman will proceed.
Mr. Knott—I was remarking, sir, upon these vast “wheat fields”
represented on this map in the immediate neighborhood of the
buffaloes and Piegans, and was about to say that the idea of there
being these immense wheat fields in the very heart of a wilderness,
hundreds and hundreds of miles beyond the utmost verge of
civilization, may appear to some gentlemen as rather incongruous, as
rather too great a strain on the “blankets” of veracity. But to my mind
there is no difficulty in the matter whatever. The phenomenon is very
easily accounted for. It is evident, sir, that the Piegans sowed that
wheat there and ploughed it in with buffalo bulls. Now, sir, this
fortunate combination of buffaloes and Piegans, considering their
relative positions to each other and to Duluth, as they are arranged
on this map, satisfies me that Duluth is destined to be the best
market of the world. Here, you will observe, (pointing to the map),
are the buffaloes, directly between the Piegans and Duluth; and here,
right on the road to Duluth, are the Creeks. Now, sir, when the
buffaloes are sufficiently fat from grazing on those immense wheat
fields, you see it will be the easiest thing in the world for the Piegans
to drive them on down, stay all night with their friends, the Creeks,
and go into Duluth in the morning. I think I see them, now, sir, a vast
herd of buffaloes, with their heads down, their eyes glaring, their
nostrils dilated, their tongues out, and their tails curled over their
backs, tearing along toward Duluth, with about a thousand Piegans
on their grass-bellied ponies, yelling at their heels! On they come!
And as they sweep past the Creeks, they join in the chase, and away
they all go, yelling, bellowing, ripping and tearing along, amid clouds
of dust, until the last buffalo is safely penned in the stock-yards at
Duluth.
Sir, I might stand here for hours and hours, and expatiate with
rapture upon the gorgeous prospects of Duluth, as depicted upon this
map. But human life is too short, and the time of this house far too
valuable to allow me to linger longer upon this delightful theme. I
think every gentleman upon this floor is as well satisfied as I am that
Duluth is destined to become the commercial metropolis of the
universe and that this road should be built at once. I am fully
persuaded that no patriotic representative of the American people,
who has a proper appreciation of the associated glories of Duluth and
the St. Croix, will hesitate a moment that every able-bodied female in
the land, between the ages of eighteen and forty-five, who is in favor
of “woman’s rights,” should be drafted and set to work upon this
great work without delay. Nevertheless, sir, it grieves my very soul to
be compelled to say that I cannot vote for the grant of lands provided
for in this bill.
Ah, sir, you can have no conception of the poignancy of my
anguish that I am deprived of that blessed privilege! There are two
insuperable obstacles in the way. In the first place my constituents,
for whom I am acting here, have no more interest in this road than
they have in the great question of culinary taste now, perhaps,
agitating the public mind of Dominica, as to whether the illustrious
commissioners, who recently left this capital for that free and
enlightened republic, would be better fricasseed, boiled, or roasted,
and, in the second place, these lands, which I am asked to give away,
alas, are not mine to bestow! My relation to them is simply that of
trustee to an express trust. And shall I ever betray that trust? Never,
sir! Rather perish Duluth! Perish the paragon of cities! Rather let the
freezing cyclones of the bleak northwest bury it forever beneath the
eddying sands of the raging St. Croix.
Henry Carey’s Speech on the Rates of
Interest.
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