Gastric leiomyosarcoma and diagnostic pitfalls: a case report

Abstract Background Since the advent of immunohistochemistry for the diagnosis of stromal tumours, the incidence of leiomyosarcomas has significantly decreased. Nowadays, gastric leiomyosarcoma is an exceptionally rare tumour. We report the second case in the English literature of gastric leiomyosar...

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Main Authors: Anis Hasnaoui, Raja Jouini, Dhafer Haddad, Haithem Zaafouri, Ahmed Bouhafa, Anis Ben Maamer, Ehsen Ben Brahim
Format: Article
Language:English
Published: BMC 2018-08-01
Series:BMC Surgery
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12893-018-0393-4
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author Anis Hasnaoui
Raja Jouini
Dhafer Haddad
Haithem Zaafouri
Ahmed Bouhafa
Anis Ben Maamer
Ehsen Ben Brahim
author_facet Anis Hasnaoui
Raja Jouini
Dhafer Haddad
Haithem Zaafouri
Ahmed Bouhafa
Anis Ben Maamer
Ehsen Ben Brahim
author_sort Anis Hasnaoui
collection DOAJ
description Abstract Background Since the advent of immunohistochemistry for the diagnosis of stromal tumours, the incidence of leiomyosarcomas has significantly decreased. Nowadays, gastric leiomyosarcoma is an exceptionally rare tumour. We report the second case in the English literature of gastric leiomyosarcoma revealed with massive bleeding and hemodynamic instability and diagnostic pitfalls that we encountered. Case presentation A 63-year-old woman, with 2 years’ history of dizziness and weakness probably related to an anaemic syndrome, presented to the emergency room with hematemesis, melena and hemodynamic instability. On examination, she had conjunctival pallor with reduced general condition, blood pressure of 90/45 mmHg and a pulse between 110 and 120 beats per minute. On digital rectal examination, she had melena. Laboratory blood tests revealed a haemoglobin level at 38 g/L. The patient was admitted to the intensive care department. After initial resuscitation, transfusion and intravenous Omeprazole continuous infusion, her condition was stabilized. She underwent upper gastrointestinal endoscopy showing a tumour of the cardia, protruding in the lumen with mucosal ulceration and clots in the stomach. Biopsies were taken. Histological examination showed interlacing bundles of spindle cells, ill-defined cell borders, elongated hyperchromatic nuclei with marked pleomorphism and paranuclear vacuolization. Immunohistochemistry showed positivity for Vimentine, a strong and diffuse immunoreactivity for smooth muscle actin (SMA). Immunoreactivities for KIT and DOG1 were doubtful. Computed tomography scan revealed a seven-cm tumour of the cardia, without adenopathy or liver metastasis. The patient underwent laparotomy. A total gastrectomy was performed without lymphadenectomy. Post-operative course was uneventful. Histological examination of the tumour specimen found the same features as preoperative biopsies with negative margins. We solicited a second opinion of an expert in a reference centre for sarcomas in France, who confirmed the diagnosis of a high grade gastric leiomyosarcoma. Conclusion Gastric leiomyosarcoma is a rare tumour. Diagnosis is based on histological examination with immunohistochemistry, which could be sometimes confusing like in our case. The validation of a pathological expert is recommended.
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spelling doaj.art-26528aa1471a4a86a0ff98a698c9022d2022-12-22T01:56:23ZengBMCBMC Surgery1471-24822018-08-011811510.1186/s12893-018-0393-4Gastric leiomyosarcoma and diagnostic pitfalls: a case reportAnis Hasnaoui0Raja Jouini1Dhafer Haddad2Haithem Zaafouri3Ahmed Bouhafa4Anis Ben Maamer5Ehsen Ben Brahim6Department of General Surgery, Habib Thameur Hospital, Tunis El Manar UniversityDepartment of Histopathology and Cytology, Habib Thameur Hospital, Tunis El Manar UniversityDepartment of General Surgery, Habib Thameur Hospital, Tunis El Manar UniversityDepartment of General Surgery, Habib Thameur Hospital, Tunis El Manar UniversityDepartment of General Surgery, Habib Thameur Hospital, Tunis El Manar UniversityDepartment of General Surgery, Habib Thameur Hospital, Tunis El Manar UniversityDepartment of Histopathology and Cytology, Habib Thameur Hospital, Tunis El Manar UniversityAbstract Background Since the advent of immunohistochemistry for the diagnosis of stromal tumours, the incidence of leiomyosarcomas has significantly decreased. Nowadays, gastric leiomyosarcoma is an exceptionally rare tumour. We report the second case in the English literature of gastric leiomyosarcoma revealed with massive bleeding and hemodynamic instability and diagnostic pitfalls that we encountered. Case presentation A 63-year-old woman, with 2 years’ history of dizziness and weakness probably related to an anaemic syndrome, presented to the emergency room with hematemesis, melena and hemodynamic instability. On examination, she had conjunctival pallor with reduced general condition, blood pressure of 90/45 mmHg and a pulse between 110 and 120 beats per minute. On digital rectal examination, she had melena. Laboratory blood tests revealed a haemoglobin level at 38 g/L. The patient was admitted to the intensive care department. After initial resuscitation, transfusion and intravenous Omeprazole continuous infusion, her condition was stabilized. She underwent upper gastrointestinal endoscopy showing a tumour of the cardia, protruding in the lumen with mucosal ulceration and clots in the stomach. Biopsies were taken. Histological examination showed interlacing bundles of spindle cells, ill-defined cell borders, elongated hyperchromatic nuclei with marked pleomorphism and paranuclear vacuolization. Immunohistochemistry showed positivity for Vimentine, a strong and diffuse immunoreactivity for smooth muscle actin (SMA). Immunoreactivities for KIT and DOG1 were doubtful. Computed tomography scan revealed a seven-cm tumour of the cardia, without adenopathy or liver metastasis. The patient underwent laparotomy. A total gastrectomy was performed without lymphadenectomy. Post-operative course was uneventful. Histological examination of the tumour specimen found the same features as preoperative biopsies with negative margins. We solicited a second opinion of an expert in a reference centre for sarcomas in France, who confirmed the diagnosis of a high grade gastric leiomyosarcoma. Conclusion Gastric leiomyosarcoma is a rare tumour. Diagnosis is based on histological examination with immunohistochemistry, which could be sometimes confusing like in our case. The validation of a pathological expert is recommended.http://link.springer.com/article/10.1186/s12893-018-0393-4LeiomyosarcomaGastricBleedingH-caldesmonKITDOG1
spellingShingle Anis Hasnaoui
Raja Jouini
Dhafer Haddad
Haithem Zaafouri
Ahmed Bouhafa
Anis Ben Maamer
Ehsen Ben Brahim
Gastric leiomyosarcoma and diagnostic pitfalls: a case report
BMC Surgery
Leiomyosarcoma
Gastric
Bleeding
H-caldesmon
KIT
DOG1
title Gastric leiomyosarcoma and diagnostic pitfalls: a case report
title_full Gastric leiomyosarcoma and diagnostic pitfalls: a case report
title_fullStr Gastric leiomyosarcoma and diagnostic pitfalls: a case report
title_full_unstemmed Gastric leiomyosarcoma and diagnostic pitfalls: a case report
title_short Gastric leiomyosarcoma and diagnostic pitfalls: a case report
title_sort gastric leiomyosarcoma and diagnostic pitfalls a case report
topic Leiomyosarcoma
Gastric
Bleeding
H-caldesmon
KIT
DOG1
url http://link.springer.com/article/10.1186/s12893-018-0393-4
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AT rajajouini gastricleiomyosarcomaanddiagnosticpitfallsacasereport
AT dhaferhaddad gastricleiomyosarcomaanddiagnosticpitfallsacasereport
AT haithemzaafouri gastricleiomyosarcomaanddiagnosticpitfallsacasereport
AT ahmedbouhafa gastricleiomyosarcomaanddiagnosticpitfallsacasereport
AT anisbenmaamer gastricleiomyosarcomaanddiagnosticpitfallsacasereport
AT ehsenbenbrahim gastricleiomyosarcomaanddiagnosticpitfallsacasereport