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伴有非典型分化性神经内分泌分化的无色素性恶性黑色素瘤:一例罕见的肛门直肠出血病例报告

Amelanotic Malignant Melanoma With Atypical Divergent Neuroendocrine Differentiation: A Report of an Unusual and Rare Case of Anorectal Bleeding.

作者信息

Mg Shamiliprabha, Cd Anand, Verma Supriya, S Nivethitha, John Jaison J

机构信息

Department of Pathology, Sri Ramaswamy Memorial (SRM) Medical College Hospital and Research Centre, SRM Institute of Science and Technology (SRMIST), Chengalpattu, IND.

出版信息

Cureus. 2024 Aug 14;16(8):e66905. doi: 10.7759/cureus.66905. eCollection 2024 Aug.

Abstract

Melanocytes located between the anal transition zone and the dentate line of the anal canal can give rise to the uncommon malignant tumor known as anal melanoma. It has a fast-paced clinical course and can masquerade as several common anorectal symptoms, such as hemorrhoids or rectal ulcers. In melanoma, divergent differentiation is a very uncommon phenomenon. The diagnosis of melanoma is difficult with histopathology sections alone (hematoxylin and eosin, H&E). Special stains and ancillary immunohistochemistry investigations are useful in these situations. A 60-year-old female patient presented to the surgical outpatient department with complaints of anorectal bleeding. After clinical evaluation, a growth in the anorectal region was identified, and a biopsy was taken from the growth. Histopathological and subsequent immunohistochemical analysis of the biopsy material was done at the Department of Pathology. A diagnosis of amelanotic melanoma with atypical and divergent neuroendocrine differentiation involving the anorectal region was rendered. Histologically, this tumor showed extremely pleomorphic polygonal to elongated spindle cells that co-expressed neuroendocrine markers and were positive for S100, HMB-45, and Melan-A. This case presented many diagnostic challenges at both the histomorphological level and the immunohistochemical expression profile analysis. We will go into great depth regarding the diagnostic challenges in this instance and provide an outline of our approach. The immunohistochemical and prognostic importance of this case will also be covered.

摘要

位于肛管肛门移行区和齿状线之间的黑素细胞可引发一种罕见的恶性肿瘤,即肛门黑色素瘤。其临床病程进展迅速,可伪装成多种常见的肛肠症状,如痔疮或直肠溃疡。在黑色素瘤中,分化异常是一种非常罕见的现象。仅靠组织病理学切片(苏木精和伊红染色,H&E)很难诊断黑色素瘤。在这些情况下,特殊染色和辅助免疫组织化学检查很有用。一名60岁女性患者因肛肠出血到外科门诊就诊。经过临床评估,发现肛肠区域有一个肿物,并对该肿物进行了活检。病理科对活检材料进行了组织病理学及后续免疫组织化学分析。诊断为累及肛肠区域的无色素性黑色素瘤伴非典型和异常神经内分泌分化。组织学上,该肿瘤表现为极度多形性的多边形至细长梭形细胞,这些细胞共表达神经内分泌标志物,且S100、HMB-45和Melan-A呈阳性。该病例在组织形态学水平和免疫组织化学表达谱分析方面都面临许多诊断挑战。我们将深入探讨该病例的诊断挑战,并概述我们的诊断方法。还将阐述该病例的免疫组织化学及预后意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c45/11401631/24f474e3fae6/cureus-0016-00000066905-i01.jpg

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