Butta Shristi, Chakraborty Shivam, Basu Keya, Islam Ayesha
Oncopathology, Institute of Post-Graduate Medical Education and Research (IPGMER) and Seth Sukhlal Karnani Memorial (SSKM) Hospital, Kolkata, IND.
Pathology, Institute of Post-Graduate Medical Education and Research (IPGMER) and Seth Sukhlal Karnani Memorial (SSKM) Hospital, Kolkata, IND.
Cureus. 2024 Oct 30;16(10):e72690. doi: 10.7759/cureus.72690. eCollection 2024 Oct.
A chondroid syringoma is a rare primary benign skin adnexal tumor with distinct histomorphology. However, extensive metaplastic bone formation within the tumor can raise diagnostic concerns. Further, the eyelid is quite a rare site of involvement of this tumor. Herein, we report a case of a chondroid syringoma with metaplastic bone formation involving the right upper eyelid in a 60-year-old female patient. The Ki67 labeling index was low. On follow-up for 36 months, no recurrence was noted. Acquaintance with the diverse histomorphological and clinical presentation of this tumor can prevent major diagnostic pitfalls.
软骨样汗腺腺瘤是一种罕见的原发性皮肤附属器良性肿瘤，具有独特的组织形态学特征。然而，肿瘤内广泛的化生骨形成可能会引发诊断方面的疑虑。此外，该肿瘤累及眼睑的情况相当罕见。在此，我们报告一例60岁女性患者，其右上眼睑发生了伴有化生骨形成的软骨样汗腺腺瘤。Ki67标记指数较低。随访36个月，未见复发。熟悉该肿瘤多样的组织形态学和临床表现可避免重大的诊断失误。
