Liposarcoma laboratory findings: Difference between revisions

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==Overview==
==Overview==
A biopsy of the liposarcoma will give the definitive diagnosis and the histopathological subtype of liposarcoma.  Other laboratory finding include anemia, due to GI bleeding, and increased [[BUN]] and [[creatinine]] in case of obstructive nephropathy.
The definitive diagnosis of liposarcoma is made by biopsy, which also provides histopathological classification of the liposarcoma's subtype.  Other pertinent laboratory finding include anemia and elevated BUN due to GI bleeding and elevated creatinine among patients with obstructive nephropathy.


==Laboratory Findings==
==Laboratory Findings==
===Biopsy===
===Biopsy===
Although imaging assists in the diagnosis of liposarcoma, a biopsy is needed to confirm the disease and determine the histopathological subtype of liposarcoma.  
Although imaging may be helpful in the diagnosis of liposarcoma, the optimal method for diagnosis of liposarcoma is by biopsy. A biopsy also provides important histopathological information requires to identify the subtype of the liposarcoma.


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| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" | Atypical Lipomatous Neoplasm (ALN)/Well-Differentiated Liposarcoma (WDL)
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" | Atypical Lipomatous Neoplasm (ALN)/Well-Differentiated Liposarcoma (WDL)
| style="padding: 5px 5px; background: #F5F5F5;" | 4 subtypes: lipoma-like, sclerosing, spindle cell and inflammatory. Multivacuolated lipoblasts and spindle cells with a hyperchromatic nuclei.  Fibrotic areas and atypical stroma cells may be observed.  
| style="padding: 5px 5px; background: #F5F5F5;" | 4 subtypes:<br>*Lipoma-like<br>*Sclerosing<br>*Spindle cell<br>*Inflammatory<br> Multivacuolated lipoblasts and spindle cells with hyperchromatic nuclei are often observedOther findings include fibrotic areas and atypical stroma cells.
|-
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" | Dedifferentiated Liposarcoma
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" | De-differentiated Liposarcoma
| style="padding: 5px 5px; background: #F5F5F5;" | Abrupt transition from a low-grade to a high-grade differentiation within the same mass of well-differentiated liposarcoma.
| style="padding: 5px 5px; background: #F5F5F5;" | Abrupt transition from a low-grade to a high-grade differentiation within the same mass of a well-differentiated liposarcoma.
|-
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" | Myxoid Liposarcoma
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" | Myxoid liposarcoma
| style="padding: 5px 5px; background: #F5F5F5;" |Multinodular mass with round cells, hyaluronic acid matrix. High cellularity at the periphery and low cellularity inside the mass. Mitotic activity is normal and the nuclei is normochromatic.  
| style="padding: 5px 5px; background: #F5F5F5;" |Multinodular mass with round cells and hyaluronic acid matrix. High cellularity at the periphery and low cellularity at the center of the mass. Mitotic activity is normal and the nuclei are normochromatic.  
|-
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" | Pleomorphic Liposarcoma
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" | Pleomorphic liposarcoma
| style="padding: 5px 5px; background: #F5F5F5;" | Pleomorphic lipoblasts with hyperchromatic nuclei, acidophilic cytoplasm and eosinophilic hyaline globules;  spinde cells and multinucleated giant cells may be observed.  
| style="padding: 5px 5px; background: #F5F5F5;" | Pleomorphic lipoblasts with hyperchromatic nuclei, acidophilic cytoplasm, and eosinophilic hyaline globules. Spindle cells and multinucleated giant cells may be observed.  
|-
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" | Mixed-type Liposarcoma
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" | Mixed-type Liposarcoma
| style="padding: 5px 5px; background: #F5F5F5;" | Mixed features of myxoid, pleomorphic and well-differentiated liposarcoma.  
| style="padding: 5px 5px; background: #F5F5F5;" | Mixed features of myxoid, pleomorphic, and well-differentiated liposarcoma.  
|-
|-
| style="padding: 5px 5px; background: #F5F5F5;" colspan=2| <small>Table adapted from Fletcher C.D.M., Unni K.K., Mertens F. (Eds.): WHO Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone<ref>{{cite book | last = Fletcher | first = Christopher | title = Pathology and genetics of tumours of soft tissue and bone | publisher = IARC Press | location = Lyon | year = 2002 | isbn = 9283224132 }}</ref> and Enzinger and Weiss's Soft Tissue Tumors , 6th Edition <ref>{{cite book | last = Goldblum | first = John | title = Enzinger and Weiss's soft tissue tumors | publisher = Saunders/Elsevier | location = Philadelphia, PA | year = 2014 | isbn = 978-0-323-08834-3 }}</ref> </small>
| style="padding: 5px 5px; background: #F5F5F5;" colspan=2| <small>Table adapted from Fletcher CDM, Unni KK, Mertens F, eds. World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone. Geneva:IARC Press; 2002<ref>{{cite book | last = Fletcher | first = Christopher | title = Pathology and genetics of tumours of soft tissue and bone | publisher = IARC Press | location = Lyon | year = 2002 | isbn = 9283224132 }}</ref> and Enzinger and Weiss's Soft Tissue Tumors , 6th Edition <ref>{{cite book | last = Goldblum | first = John | title = Enzinger and Weiss's soft tissue tumors | publisher = Saunders/Elsevier | location = Philadelphia, PA | year = 2014 | isbn = 978-0-323-08834-3 }}</ref> </small>
|-
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===Laboratory Tests===
===Laboratory Tests===
*There are no specific laboratory test findings for the diagnosis of liposarcoma.  
*There are no specific laboratory tests for the diagnosis of liposarcoma.  
*In cases of [[ureter]] or [[kidney]] involvement, an elevated [[creatinine]] and [[BUN]] may be seen.  
*Patients with[[ureteral]] or [[renal]] involvement, an elevated [[creatinine]] may be observed.
*[[Anemia]] may be present, specially if there is [[bleeding]] associated with the liposarcoma. <ref name="NennstielMollenhauer2014">{{cite journal|last1=Nennstiel|first1=Simon|last2=Mollenhauer|first2=Martin|last3=Schlag|first3=Christoph|last4=Becker|first4=Valentin|last5=Neu|first5=Bruno|last6=Hüser|first6=Norbert|last7=Gertler|first7=Ralf|last8=Schmid|first8=Roland M.|last9=von Delius|first9=Stefan|title=Small Bowel Pleomorphic Liposarcoma: A Rare Cause of Gastrointestinal Bleeding|journal=Case Reports in Gastrointestinal Medicine|volume=2014|year=2014|pages=1–4|issn=2090-6528|doi=10.1155/2014/391871}}</ref>
*[[Anemia]] and elevated BUN may be present among patients with liposarcoma assoicated with GI bleeding.<ref name="NennstielMollenhauer2014">{{cite journal|last1=Nennstiel|first1=Simon|last2=Mollenhauer|first2=Martin|last3=Schlag|first3=Christoph|last4=Becker|first4=Valentin|last5=Neu|first5=Bruno|last6=Hüser|first6=Norbert|last7=Gertler|first7=Ralf|last8=Schmid|first8=Roland M.|last9=von Delius|first9=Stefan|title=Small Bowel Pleomorphic Liposarcoma: A Rare Cause of Gastrointestinal Bleeding|journal=Case Reports in Gastrointestinal Medicine|volume=2014|year=2014|pages=1–4|issn=2090-6528|doi=10.1155/2014/391871}}</ref>
* The level of [[D-dim]]er has been studied as a marker for the differential diagnosis of [[lipoma]] and well-differentiated liposarcoma, the latter having higher levels of [[D-dimer]].<ref>{{Cite journal
* The level of [[D-dimer]] has been studied as a marker for the differential diagnosis of [[lipoma]] and well-differentiated liposarcoma. Results have demonstrated that liposarcoma may have increased levels of D-dimer compared to lipoma.<ref>{{Cite journal
| author = [[Akira Yoshiyama]], [[Takeshi Morii]], [[Takashi Tajima]], [[Takayuki Aoyagi]], [[Keita Honya]], [[Kazuo Mochizuki]], [[Kazuhiko Satomi]] & [[Shoichi Ichimura]]
| author = [[Akira Yoshiyama]], [[Takeshi Morii]], [[Takashi Tajima]], [[Takayuki Aoyagi]], [[Keita Honya]], [[Kazuo Mochizuki]], [[Kazuhiko Satomi]] & [[Shoichi Ichimura]]
  | title = D-dimer Levels in the Differential Diagnosis Between Lipoma and Well-differentiated Liposarcoma
  | title = D-dimer Levels in the Differential Diagnosis Between Lipoma and Well-differentiated Liposarcoma

Revision as of 19:34, 23 September 2014

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Alejandro Lemor, M.D. [2]

Overview

The definitive diagnosis of liposarcoma is made by biopsy, which also provides histopathological classification of the liposarcoma's subtype. Other pertinent laboratory finding include anemia and elevated BUN due to GI bleeding and elevated creatinine among patients with obstructive nephropathy.

Laboratory Findings

Biopsy

Although imaging may be helpful in the diagnosis of liposarcoma, the optimal method for diagnosis of liposarcoma is by biopsy. A biopsy also provides important histopathological information requires to identify the subtype of the liposarcoma.

Subtype Findings
Atypical Lipomatous Neoplasm (ALN)/Well-Differentiated Liposarcoma (WDL) 4 subtypes:
*Lipoma-like
*Sclerosing
*Spindle cell
*Inflammatory
Multivacuolated lipoblasts and spindle cells with hyperchromatic nuclei are often observed. Other findings include fibrotic areas and atypical stroma cells.
De-differentiated Liposarcoma Abrupt transition from a low-grade to a high-grade differentiation within the same mass of a well-differentiated liposarcoma.
Myxoid liposarcoma Multinodular mass with round cells and hyaluronic acid matrix. High cellularity at the periphery and low cellularity at the center of the mass. Mitotic activity is normal and the nuclei are normochromatic.
Pleomorphic liposarcoma Pleomorphic lipoblasts with hyperchromatic nuclei, acidophilic cytoplasm, and eosinophilic hyaline globules. Spindle cells and multinucleated giant cells may be observed.
Mixed-type Liposarcoma Mixed features of myxoid, pleomorphic, and well-differentiated liposarcoma.
Table adapted from Fletcher CDM, Unni KK, Mertens F, eds. World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone. Geneva:IARC Press; 2002[1] and Enzinger and Weiss's Soft Tissue Tumors , 6th Edition [2]


Well Differentiated Liposarcoma. Image courtesy of Wikimedia Commons.
Dedifferentiated Liposarcoma. Image courtesy of Wikimedia Commons.
Dedifferentiated Liposarcoma. Image courtesy of Wikimedia Commons.
Dedifferentiated Liposarcoma. Image courtesy of Wikimedia Commons.
Dedifferentiated Liposarcoma. Image courtesy of Wikimedia Commons.

Laboratory Tests

  • There are no specific laboratory tests for the diagnosis of liposarcoma.
  • Patients withureteral or renal involvement, an elevated creatinine may be observed.
  • Anemia and elevated BUN may be present among patients with liposarcoma assoicated with GI bleeding.[3]
  • The level of D-dimer has been studied as a marker for the differential diagnosis of lipoma and well-differentiated liposarcoma. Results have demonstrated that liposarcoma may have increased levels of D-dimer compared to lipoma.[4]

References

  1. Fletcher, Christopher (2002). Pathology and genetics of tumours of soft tissue and bone. Lyon: IARC Press. ISBN 9283224132.
  2. Goldblum, John (2014). Enzinger and Weiss's soft tissue tumors. Philadelphia, PA: Saunders/Elsevier. ISBN 978-0-323-08834-3.
  3. Nennstiel, Simon; Mollenhauer, Martin; Schlag, Christoph; Becker, Valentin; Neu, Bruno; Hüser, Norbert; Gertler, Ralf; Schmid, Roland M.; von Delius, Stefan (2014). "Small Bowel Pleomorphic Liposarcoma: A Rare Cause of Gastrointestinal Bleeding". Case Reports in Gastrointestinal Medicine. 2014: 1–4. doi:10.1155/2014/391871. ISSN 2090-6528.
  4. Akira Yoshiyama, Takeshi Morii, Takashi Tajima, Takayuki Aoyagi, Keita Honya, Kazuo Mochizuki, Kazuhiko Satomi & Shoichi Ichimura (2014). "D-dimer Levels in the Differential Diagnosis Between Lipoma and Well-differentiated Liposarcoma". Anticancer research. 34 (9): 5181–5185. PMID 25202112. Unknown parameter |month= ignored (help)


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