Evidence map›Paper›PMID 39566431›Full record

ArticleInternational journal of surgery case reports2024

Chondroid syringoma on the nasal wing: A case report in a 22-year-old male.

Bakri Roumi Jamal, Lana Sabbagh, Aya Asfari, Julie Khayat, Alaa Alzakri, Silva Ishkhanian

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Article in International journal of surgery case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Bakri Roumi JamalFaculty of Medicine, University of Aleppo, Aleppo, Syria.
Lana SabbaghFaculty of Medicine, University of Aleppo, Aleppo, Syria. Electronic address: lanasabbagh88@gmail.com.
Aya AsfariFaculty of Medicine, University of Aleppo, Aleppo, Syria.
Julie KhayatFaculty of Medicine, University of Aleppo, Aleppo, Syria.
Alaa AlzakriDepartment of Dermatology, Faculty of Medicine, University of Aleppo, Aleppo, Syria.
Silva IshkhanianDepartment of Dermatology, Faculty of Medicine, University of Aleppo, Aleppo, Syria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introduction and importanceChondroid syringoma also referred to as a mixed tumor, is a benign and rare tumor originating from apocrine or eccrine sweat glands; it predominantly affects middle-aged men. While fine-needle aspiration cytology can aid in diagnosis, histological confirmation remains essential due to the potential for misdiagnosis. CASE PRESENTATION: A-22-year-old male who presented with a solitary, slow-growing, painless, erythematous nodule on the right nasal wing that had been present for 1 year, which was misdiagnosed as an epidermal cyst. an excisional biopsy was performed and showed in histological examination foci of myxoid to cartilaginous lakes associated with glandular structures. CLINICAL DISCUSSION: Chondroid syringoma characterized by mesenchymal and epithelial components. Typically presenting as a painless nodule on the head and neck, CS can be misdiagnosed due to overlapping features with other lesions. Diagnosis involves fine-needle aspiration cytology and histological confirmation. The primary treatment is surgical excision.

conclusionChondroid syringoma has distinctive histological characteristics, which include myxoid to cartilaginous components alongside glandular structures, these features are essential for accurate differentiation from other neoplasms. Surgical excision with an adequate margin of normal tissue is the recommended treatment approach to ensure complete removal and minimize recurrence.

Indexed as

BenignBiopsyCase reportChondroid syringomaMixed tumorNodule

Identifiers

PMID39566431
PMCPMC11747603

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