Primary hepatic leiomyosarcoma. A case report

Primary hepatic leiomyosarcoma is extremely rare among cases of liver tumors in adults, with an incidence of 0.1 and 1%. This paper describes the case of a 55 year-old man with a clinical evolution of five months consisting of abdominal pain, a large hard lump, weight loss, shortness of breath and f...

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Main Authors: Jhon Mauricio Coronel Ruilova, José Enrique Zúñiga Bohórquez, Lincoln Alexander Cabezas Barragán
Format: Article
Language:English
Published: Universidad Nacional de Colombia 2016-07-01
Series:Case Reports
Subjects:
Online Access:https://revistas.unal.edu.co/index.php/care/article/view/58180
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spelling doaj-34001dbe3c66411892296df179cee5e62020-11-25T00:38:35ZengUniversidad Nacional de ColombiaCase Reports2462-85222016-07-0122354344679Primary hepatic leiomyosarcoma. A case reportJhon Mauricio Coronel Ruilova0José Enrique Zúñiga Bohórquez1Lincoln Alexander Cabezas Barragán2Hospital Luis VernazaHospital Luis Vernaza, Universidad de Especialidades Espíritu Santo GuayaquilHospital Luis Vernaza,Primary hepatic leiomyosarcoma is extremely rare among cases of liver tumors in adults, with an incidence of 0.1 and 1%. This paper describes the case of a 55 year-old man with a clinical evolution of five months consisting of abdominal pain, a large hard lump, weight loss, shortness of breath and fever. A three-phase computed tomography (CT) showed a hypercaptive mass at its periphery during hypodense arterial phase at its center, located in segments VI and VI, without a plane of separation of the liver. Due to the symptoms, the patient underwent an exploratory laparotomy, finding a cerebroid mass of 40 x 40 cm; a lumpectomy without hepatectomy was performed, leaving free surgical margins. The diagnosis was largely made through a histopathological assessment, finding stromal multinucleated pleomorphic forms, desmin (+), SMA (smooth muscle actin) and MSA (muscle specific actin) (+), Ki67 (+) and negative for S100 (protein S100) and CD117 antibody, which confirmed the high grade pleomorphic leiomyosarcoma diagnosis. The patient was discharged 16 days after admission once his condition improved, and was referred to the oncology department for adjuvant chemotherapy. Given the size of the mass, the prognosis was bleak, which left surgery as the only option to offer survival expectations through regulated or "atypical" hepatectomies along with safety margins and liver transplantation. With this in mind, the first option was chosen; six months after surgery, with clinical improvement and adjuvant therapy, the patient, still with unfavorable prognosis, remained stable attending multidisciplinary medical management controls.https://revistas.unal.edu.co/index.php/care/article/view/58180LeiomyosarcomaSarcomaHepatic neoplasmsHepatectomySmooth muscle actin.
collection DOAJ
language English
format Article
sources DOAJ
author Jhon Mauricio Coronel Ruilova
José Enrique Zúñiga Bohórquez
Lincoln Alexander Cabezas Barragán
spellingShingle Jhon Mauricio Coronel Ruilova
José Enrique Zúñiga Bohórquez
Lincoln Alexander Cabezas Barragán
Primary hepatic leiomyosarcoma. A case report
Case Reports
Leiomyosarcoma
Sarcoma
Hepatic neoplasms
Hepatectomy
Smooth muscle actin.
author_facet Jhon Mauricio Coronel Ruilova
José Enrique Zúñiga Bohórquez
Lincoln Alexander Cabezas Barragán
author_sort Jhon Mauricio Coronel Ruilova
title Primary hepatic leiomyosarcoma. A case report
title_short Primary hepatic leiomyosarcoma. A case report
title_full Primary hepatic leiomyosarcoma. A case report
title_fullStr Primary hepatic leiomyosarcoma. A case report
title_full_unstemmed Primary hepatic leiomyosarcoma. A case report
title_sort primary hepatic leiomyosarcoma. a case report
publisher Universidad Nacional de Colombia
series Case Reports
issn 2462-8522
publishDate 2016-07-01
description Primary hepatic leiomyosarcoma is extremely rare among cases of liver tumors in adults, with an incidence of 0.1 and 1%. This paper describes the case of a 55 year-old man with a clinical evolution of five months consisting of abdominal pain, a large hard lump, weight loss, shortness of breath and fever. A three-phase computed tomography (CT) showed a hypercaptive mass at its periphery during hypodense arterial phase at its center, located in segments VI and VI, without a plane of separation of the liver. Due to the symptoms, the patient underwent an exploratory laparotomy, finding a cerebroid mass of 40 x 40 cm; a lumpectomy without hepatectomy was performed, leaving free surgical margins. The diagnosis was largely made through a histopathological assessment, finding stromal multinucleated pleomorphic forms, desmin (+), SMA (smooth muscle actin) and MSA (muscle specific actin) (+), Ki67 (+) and negative for S100 (protein S100) and CD117 antibody, which confirmed the high grade pleomorphic leiomyosarcoma diagnosis. The patient was discharged 16 days after admission once his condition improved, and was referred to the oncology department for adjuvant chemotherapy. Given the size of the mass, the prognosis was bleak, which left surgery as the only option to offer survival expectations through regulated or "atypical" hepatectomies along with safety margins and liver transplantation. With this in mind, the first option was chosen; six months after surgery, with clinical improvement and adjuvant therapy, the patient, still with unfavorable prognosis, remained stable attending multidisciplinary medical management controls.
topic Leiomyosarcoma
Sarcoma
Hepatic neoplasms
Hepatectomy
Smooth muscle actin.
url https://revistas.unal.edu.co/index.php/care/article/view/58180
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