Virginia Tech Carilion School of Medicine, Roanoke, VA.
Dermatology Section, Department of Internal Medicine, Virginia Tech Carilion School of Medicine, Roanoke, VA.
Am J Dermatopathol. 2021 Dec 1;43(12):e254-e258. doi: 10.1097/DAD.0000000000001975.
Oncocytomas are benign neoplasms that are most often found in the salivary glands and kidneys. Ocular oncocytoma typically present as an asymptomatic dark blue papule on the lacrimal caruncle. Histologically, the tumor is composed of oncocytes, cells notable for eosinophilic cytoplasmic granules representing large quantities of dysfunctional mitochondria. The neoplastic proliferation may be partially or totally encapsulated and may be surrounded by myoepithelial cells. Discussed is the pathophysiology and histopathology of an ocular oncocytoma from the right lacrimal caruncle of a 68-year-old man. The patient complained of a foreign body sensation and tearing associated with a purpuric 1 × 1-mm papule of the right caruncle that had been present for 6 months. An excisional biopsy showed an oxyntic neoplasm with small cystic glandular spaces associated with goblet cells and mucin, confirmed by mucicarmine stain. Given the rarity of ocular oncocytomas and presence of mucin, exclusion of an endocrine mucin-producing sweat gland carcinoma was necessary. Peripheral myoepithelial cells noted on p63 immunostaining are seen in both endocrine mucin-producing sweat gland carcinoma and oncocytomas. However, endocrine mucin-producing sweat gland carcinoma is excluded by the presence of goblet cells, the uniform oxyphilic cytoplasm of the epithelial cells, and the negative immunohistochemical staining for neuron-specific enolase, chromogranin, synaptophysin, estrogen receptor, and progesterone receptor. Complete surgical excision is the treatment of choice for oncocytomas. This case highlights the clinical and histopathological presentation of ocular oncocytomas and raises awareness of this rare entity for both the practicing dermatologist and dermatopathologist.
肾细胞癌是一种良性肿瘤,最常见于唾液腺和肾脏。眼附属器的肾细胞癌通常表现为泪阜部位无症状的深蓝色丘疹。组织学上,肿瘤由嗜酸性细胞质颗粒构成的肾嗜酸细胞瘤组成,这些颗粒代表大量功能失调的线粒体。肿瘤的增生可能部分或完全被包膜包裹,并可能被肌上皮细胞包围。讨论了一名 68 岁男性右侧泪阜眼附属器肾嗜酸细胞瘤的病理生理学和组织病理学。患者诉有异物感和流泪,伴有右侧泪阜存在 6 个月的 1×1mm 紫癜性丘疹。切除活检显示一种胃泌素瘤,伴有小的囊性腺腔,与杯状细胞和粘蛋白有关,粘蛋白卡红染色证实了这一点。鉴于眼附属器肾嗜酸细胞瘤和粘蛋白的罕见性,需要排除产生内分泌粘蛋白的汗腺癌。p63 免疫染色显示的周围肌上皮细胞在产生内分泌粘蛋白的汗腺癌和肾嗜酸细胞瘤中均可见。然而,由于存在杯状细胞、上皮细胞均匀嗜酸性细胞质和神经元特异性烯醇化酶、嗜铬粒蛋白、突触素、雌激素受体和孕激素受体免疫组织化学染色阴性,排除了产生内分泌粘蛋白的汗腺癌。完全手术切除是肾嗜酸细胞瘤的首选治疗方法。该病例突出了眼附属器肾嗜酸细胞瘤的临床和组织病理学表现,提高了皮肤科医生和皮肤病理学家对这一罕见实体的认识。