一例罕见的腹膜间皮瘤透明细胞变异

MD Nivethietha Maniam, Ming Ta Michael Lee, MD Mihir M. Shah, MD Richard Alexander
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引用次数: 0

摘要

摘要透明细胞亚型原发性恶性腹膜间皮瘤是一种罕见的恶性肿瘤,以往报道的病例很少。我们报告一位63岁的女性,她表现为腹胀,并被诊断为腹膜透明细胞间皮瘤,并转移到肝脏。患者手术切除了大于50厘米的肿块,并切除了部分肝脏和胃,术后过程平稳。腹膜间皮瘤的预后和治疗建议建立在组织学亚型和患者特异性因素的基础上,尽管它们没有明确地包括透明细胞亚型。本病例报告描述了一种罕见的腹膜间皮瘤的表现、治疗和早期结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Presentation of a Clear Cell Variant of Peritoneal Mesothelioma
Primary malignant peritoneal mesothelioma with clear cell subtype is a rare malignancy with few previously reported cases. We present a 63-year-old female who presented with abdominal distention and was diagnosed with clear cell mesothelioma of the peritoneum with an isolated metastasis to the liver. The patient underwent surgical resection of a greater than 50 cm mass with en-bloc partial liver and gastric resection with an uneventful post-operative course. There are established prognostic and treatment recommendations for peritoneal mesothelioma based on histological subtype and patient-specific factors, although they do not explicitly incorporate clear cell subtype. This case report describes the presentation, treatment and early outcome of a rare form of peritoneal mesothelioma.
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