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Case Reports
. 2023 Feb 2;15(2):e34571.
doi: 10.7759/cureus.34571. eCollection 2023 Feb.

Benign Chondroid Syringoma on Chin: A Case Report and Literature Review

Affiliations
Case Reports

Benign Chondroid Syringoma on Chin: A Case Report and Literature Review

Garima Anandani et al. Cureus. .

Abstract

Chondroid syringoma is a cutaneous adnexal tumor originating from sweat glands origin. It is rare in occurrence and usually benign, having an incidence of 0.01 to 0.098%. As these tumors are uncommon, their diagnosis is missed many times and are misdiagnosed. Hence in any case of facial skin swelling increasing slowly in size, this entity should be kept in mind as one of the possibilities and differential diagnosis. Histopathological examination of the excision biopsy gives the definitive confirmatory diagnosis. Surgically excising the swelling locally along with a surrounding normal tissue cuff is the standard treatment given which prevents recurrence. Hereby we present a 35-year-old case of facial chondroid syringoma having a focal component of eccrine hidrocystoma, keratinous cyst as well as syringocystadenoma papilliferum on the chin that was clinically suspected to be an epidermoid cyst or mucocele.

Keywords: benign skin adnexal tumour; chondroid syringoma; epithelial and mesenchymal; mixed tumour; multiple components.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. FNAC smears from the lesion show scattered nucleate and anucleate squamous cells and adnexa in keratinous background. (A) Geimsa stain 400X (B) PAP stain 400X
FNAC: Fine needle aspiration cytology, PAP: Papanicolaou
Figure 2
Figure 2. (A) The lesion was present on the chin with greyish brown overlying skin. (B) Nodular excision biopsy with greyish brown outer surface. (C) Cut section shows solid as well as cystic areas.
Figure 3
Figure 3. Microscopy shows a well-circumscribed and unencapsulated dermal tumor composed of cells arranged in solid cords, clusters as well as forming ductal structures in chondromyxoid stroma (H&E stain) (A) 40X (B) 100X (C) 200X (D) 400X
Figure 4
Figure 4. (A) Cystic component was also present forming eccrine hidrocystoma at places (H&E stain, 100 X) (B) Predominantly apocrine glands were seen with few (C) eccrine glands and (D) focal dystrophic calcification (H&E stain, 200X).
Figure 5
Figure 5. There was presence of focal (A) keratinous cysts (B) glandular secretions in lumen (C) apocrine metaplasia and (D) area of syringocystanedoma papilliferum (H&E stain, 200X).

References

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