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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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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 |
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. |
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