Shah Aekta, Rekhi Bharat, Patil Asawari
Department of Surgical Pathology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, Maharashtra, India.
Indian J Pathol Microbiol. 2021 Oct-Dec;64(4):767-770. doi: 10.4103/IJPM.IJPM_624_20.
Alveolar soft part sarcoma (ASPS) and certain perivascular epithelioid cell neoplasms (PEComas) exhibit overlapping histopathological features, including immunohistochemical expression of TFE3, as well as TFE3 gene rearrangement. PEComas with an epithelioid morphology are known to exhibit variable immunoexpression of muscle markers. At the same time, aberrant immunoreactivity of HMB45 immunostain, which is invariably, used to substantiate a diagnosis of a PEComa, has been reported in various other tumors. Herein, we discuss two rare cases of soft tissue tumors with overlapping morphological and immunohistochemical features. Case1: A 34-year-old male underwent a biopsy for a recurrent, right-sided nasal polyp. Biopsy showed polygonal tumor cells, containing prominent nucleoli, arranged in a "nesting-type"/alveolar growth pattern. Immunohistochemically, tumor cells displayed TFE3 positivity and an aberrant positivity for HMB45. Special stain (PAS-diastase) highlighted intracytoplasmic granules and crystals. Diagnosis of ASPS was offered. Furthermore, the tumor cells displayed TFE3 gene rearrangement. Case 2: A 29-year-old female underwent an aural polypectomy. Microscopic examination revealed a tumor with a "nesting-type"/alveolar arrangement of tumor cells with vacuolated cytoplasm, arranged around thin-walled blood vessels. Immunohistochemically, tumor cells were diffusely positive for HMB45 and TFE3 and focally for SMA. A diagnosis of a PEComa was offered. This report constitutes the first documentation of aberrant HMB45 immunoreactivity in case of ASPS, and one of the first reported cases of a PEComa in the ear. It emphasizes the value of integrating clinicopathological features with immunohistochemical and molecular results in differentiating two rare, but distinct soft tissue tumors with overlapping features. An exact diagnosis of both these tumor entities has therapeutic implications.
肺泡软组织肉瘤(ASPS)和某些血管周上皮样细胞肿瘤(PEComas)具有重叠的组织病理学特征,包括TFE3的免疫组化表达以及TFE3基因重排。已知具有上皮样形态的PEComas表现出肌肉标志物免疫表达的差异。同时,在各种其他肿瘤中也报道了HMB45免疫染色的异常免疫反应性,而HMB45免疫染色一直被用于证实PEComa的诊断。在此,我们讨论两例具有重叠形态学和免疫组化特征的罕见软组织肿瘤病例。病例1:一名34岁男性因右侧复发性鼻息肉接受活检。活检显示多边形肿瘤细胞,含有突出的核仁,呈“巢状”/肺泡样生长模式。免疫组化显示,肿瘤细胞TFE3阳性,HMB45呈异常阳性。特殊染色(PAS-淀粉酶)突出显示胞浆内颗粒和晶体。诊断为ASPS。此外,肿瘤细胞显示TFE3基因重排。病例2:一名29岁女性接受了耳息肉切除术。显微镜检查显示肿瘤细胞呈“巢状”/肺泡样排列,胞浆有空泡,围绕薄壁血管排列。免疫组化显示,肿瘤细胞HMB45和TFE3弥漫性阳性,平滑肌肌动蛋白(SMA)局灶性阳性。诊断为PEComa。本报告首次记录了ASPS病例中HMB45的异常免疫反应性,也是耳内PEComa的首批报道病例之一。它强调了将临床病理特征与免疫组化和分子结果相结合在鉴别两种具有重叠特征的罕见但不同的软组织肿瘤中的价值。对这两种肿瘤实体的准确诊断具有治疗意义。