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Leiomyosarcoma of the gallbladder—A case report and a review of literature

INTRODUCTION: Primary sarcomas of the gallbladder (GB) are a rare disease that were first described by Griffon and Segall in 1897. Leiomyosarcomas (LMS), as described in the case report at hand, are considered a major subgroup. PRESENTATION OF CASE: A 62-year-old female was referred to our hospital...

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Detalles Bibliográficos
Autores principales: Paasch, Christoph, Salak, Muharrem, Mairinger, Thomas, Theissig, Franz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928315/
https://www.ncbi.nlm.nih.gov/pubmed/31864148
http://dx.doi.org/10.1016/j.ijscr.2019.11.062
Descripción
Sumario:INTRODUCTION: Primary sarcomas of the gallbladder (GB) are a rare disease that were first described by Griffon and Segall in 1897. Leiomyosarcomas (LMS), as described in the case report at hand, are considered a major subgroup. PRESENTATION OF CASE: A 62-year-old female was referred to our hospital with intermittent right upper quadrant pain. A 45 mm mass arising from the neck of the GB was diagnosed by ultrasound. No distant metastases were revealed. We successfully removed the GB and the surrounding liver tissue. We also performed a lymphadenectomy of the hepatoduodenal ligament. The histopathological and immunohistochemical examination revealed an R0 resected epithelioid LMS of the GB. DISCUSSION: Our review of literature shows only 20 publications of LMS of the GB. The majority of the patients are female with an average age of 65.95 years. In a non-metastasized stage, a cholecystectomy with a wedge resection of the surrounding liver tissue, accompanied by a lymphadenectomy of the hepatoduodenal ligament, is described as a successful surgical approach. CONCLUSION: The LMS should be taken under consideration when diagnosing a tumor of the GB.