Unusual presentation of chondroid syringoma of the hand: a literature review and case report

手部软骨样汗管瘤的罕见表现:文献回顾及病例报告

阅读:1

Abstract

INTRODUCTION AND IMPORTANCE: Malignant chondroid syringoma (CS) is a sporadic skin tumor with slow growth and metastatic potential. Its presentation in the hand is uncommon, and limited cases have been reported in the literature. This case highlights an unusual presentation of malignant CS with delayed diagnosis, bone erosion, and distant metastases, adding to the sparse surgical literature on this tumor's aggressive behavior. CASE PRESENTATION: A 67-year-old male with a 5-year history of a progressively enlarging ulcerative lesion on his left hand, initially mistaken for an insect bite. The lesion caused pain, limited finger mobility, and led to fifth-digit loss. Imaging revealed soft tissue swelling, bone erosion, and multiple lytic lesions in bone. The patient underwent a ray amputation of the ring finger. Pathology confirmed malignant CS with positive S-100 and CA-9/19 markers. Despite chemotherapy and surveillance, the patient's condition worsened due to metastatic progression, resulting in death 2 years after the initial presentation. CLINICAL DISCUSSION: Malignant CS of the hand is a rare tumor with sparse literature on its aggressive behavior. It may be easily misdiagnosed as a benign chronic lesion, leading to delayed treatment. Early recognition with aggressive evaluation could allow for timely wide excision with appropriate margins and surveillance, limiting metastasis and poor prognosis. CONCLUSION: This case emphasizes the importance of considering malignant CS in chronic hand lesions with progressive bone involvement. Early diagnosis, wide local excision, and close monitoring are crucial due to the tumor's metastatic potential and poor prognosis, especially in larger or truncal tumors.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。