Literature DB >> 29225876

Asymptomatic giant retroperitoneal mass detected at a medical checkup.

Tsutomu Takeda1, Daisuke Asaoka1, Yuki Fukumura2, Sumio Watanabe1.   

Abstract

The differential diagnosis of retroperitoneal mass includes liposarcoma, leiomyosarcoma, malignant fibrous histiocytoma, neurofibroma, stromal tumor, teratoma, and lymphoma. Leiomyosarcoma is rare with poorer prognosis than other soft tissue sarcomas. Soft tissue sarcoma of retroperitoneal origin often remains asymptomatic until tumor enlargement, leading to diagnosis at advanced stages.

Entities:  

Keywords:  Leiomyosarcoma; metastasis; retroperitoneal mass

Year:  2017        PMID: 29225876      PMCID: PMC5715433          DOI: 10.1002/ccr3.1231

Source DB:  PubMed          Journal:  Clin Case Rep        ISSN: 2050-0904


Question

Multiple lung tumors were detected at a routine medical checkup at the office on a chest X‐ray in a 46‐year‐old woman. CT scanning identified a 150‐mm solid tumor with irregular density and some areas of weak enhancement in the left retroperitoneum, and multiple liver/lung/bone metastases (Figs 1 and 2). What is the clinical diagnosis?
Figure 1

Computed tomography showed a solid tumor with irregular density in the left retroperitoneum and multiple liver metastases.

Figure 2

Computed tomography and bone scintigraphy showed multiple lung and bone metastases.

Computed tomography showed a solid tumor with irregular density in the left retroperitoneum and multiple liver metastases. Computed tomography and bone scintigraphy showed multiple lung and bone metastases.

Answer

A diagnosis of leiomyosarcoma was given based on a liver biopsy showing atypical spindle cells, which were positive for smooth muscle actin (SMA) and negative for KIT, CD34, and S‐100 immunohistochemically (Fig. 3). Leiomyosarcoma is a rare tumor with poor prognosis. Leiomyosarcoma of retroperitoneal origin often remains asymptomatic until tumor enlargement 1, 2. Most of the solid retroperitoneal neoplasms are of mesodermal origin, with liposarcomas, leiomyosarcomas, and malignant fibrous histiocytomas. Other differential diagnoses are neurogenic tumors, germ cell, sex cord, and stromal tumors and lymphoid and hematologic tumors such as neurofibromas, teratomas, and lymphomas 3, 4.
Figure 3

Medium power view of the H&E section showed atypical spindle cells, which were positive for smooth muscle actin (SMA) and negative for KIT, CD34, and S‐100 immunohistochemically.

Medium power view of the H&E section showed atypical spindle cells, which were positive for smooth muscle actin (SMA) and negative for KIT, CD34, and S‐100 immunohistochemically.

Conflict of Interest

The authors state that they have no conflict of interest.

Authorship

TT: gastroenterologist, responsible for the hospitalization and outpatient follow‐up of the case, and also had the major role in writing the manuscript. DA: gastroenterologist, responsible for the hospitalization and outpatient follow‐up of the case. YF: pathologist, responsible for pathological examination. SW: Professor of Department of Gastroenterology, Juntendo University School of Medicine; had the whole supervision of the case.
  4 in total

1.  Imaging of uncommon retroperitoneal masses.

Authors:  Prabhakar Rajiah; Rakesh Sinha; Carlos Cuevas; Theodore J Dubinsky; William H Bush; Orpheus Kolokythas
Journal:  Radiographics       Date:  2011 Jul-Aug       Impact factor: 5.333

2.  Retroperitoneal sarcomas: patterns of care at diagnosis, prognostic factors and focus on main histological subtypes: a multicenter analysis of the French Sarcoma Group.

Authors:  M Toulmonde; S Bonvalot; P Méeus; E Stoeckle; O Riou; N Isambert; E Bompas; M Jafari; C Delcambre-Lair; E Saada; A Le Cesne; C Le Péchoux; J Y Blay; S Piperno-Neumann; C Chevreau; J O Bay; V Brouste; P Terrier; D Ranchère-Vince; A Neuville; A Italiano
Journal:  Ann Oncol       Date:  2014-03       Impact factor: 32.976

Review 3.  Retroperitoneal soft tissue sarcoma.

Authors:  William M Mendenhall; Robert A Zlotecki; Steven N Hochwald; Alan W Hemming; Stephen R Grobmyer; William G Cance
Journal:  Cancer       Date:  2005-08-15       Impact factor: 6.860

4.  Soft tissue tumours of the retroperitoneum.

Authors:  J F Van Roggen; P C Hogendoorn
Journal:  Sarcoma       Date:  2000
  4 in total

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