Prasad Anil, Kumar Binod, Mehta Sameer Kumar, Mishra Minakshi
Department of Pathology, Tata Main Hospital, Jamshedpur, Jharkhand, India.
Department of Dermatology, Tata Main Hospital, Jamshedpur, Jharkhand, India.
Int J Appl Basic Med Res. 2025 Jan-Mar;15(1):60-62. doi: 10.4103/ijabmr.ijabmr_363_24. Epub 2025 Jan 9.
Chondroid syringoma (CS) is a rare benign skin adnexal neoplasm. Its incidence is very low among all primary skin tumors. Diagnosing it clinically can be difficult as it closely resembles other benign salivary or adnexal neoplasms. Until now, only a few cases have been reported from the periorbital region. Clinically, it can be mistaken for epidermal cysts, but ectopic salivary glands are a close differential diagnosis. To diagnose it, a complete removal is usually required, followed by a histopathological examination. We present a unique case of a 45-year-old female patient with a CS in her right supraorbital ridge and review the pertinent literature.
软骨样汗腺腺瘤(CS)是一种罕见的皮肤附属器良性肿瘤。在所有原发性皮肤肿瘤中,其发病率极低。临床上诊断该病可能较为困难,因为它与其他良性涎腺或附属器肿瘤极为相似。迄今为止,仅少数眶周区域病例有报道。临床上,它可能被误诊为表皮样囊肿,但异位涎腺是相近的鉴别诊断对象。要诊断该病,通常需要完整切除,随后进行组织病理学检查。我们报告一例45岁女性患者右眶上嵴软骨样汗腺腺瘤的独特病例,并复习相关文献。