Department of Pathology and Lab Medicine, All India Institute of Medical Sciences, JODHPUR, INDIA.
Turk Patoloji Derg. 2022;38(1):70-72. doi: 10.5146/tjpath.2021.01534.
Granular cell tumours are uncommon acquired benign tumours of nerve sheath origin that are usually seen in the head and neck region and upper aero-digestive tract. They usually present as solitary small sized nodules in middle age. The tumour is usually benign and composed of sheets of large sized cells with abundant granular cytoplasm containing lysosomal macro-inclusions known as pustulo-ovoid bodies of Milian (POB) that represent the heterogeneity of the lysosomes. No well-established criteria for malignancy have been described for this tumour. In this article, we have discussed a rare case of granular cell tumour of the penis with its characteristic histomorphology and immunohistochemistry and relevant differential diagnosis.
颗粒细胞瘤是一种罕见的来源于神经鞘的获得性良性肿瘤,通常发生在头颈部和上呼吸道。它们通常表现为中年时的孤立性小结节。肿瘤通常为良性,由大片大细胞组成,胞质丰富,含有溶酶体大包涵体,称为米利安的脓疱状卵圆形体(POB),代表溶酶体的异质性。目前尚未为该肿瘤描述明确的恶性标准。本文讨论了一例罕见的阴茎颗粒细胞瘤,其具有特征性的组织形态学和免疫组织化学表现及相关鉴别诊断。