A rare ossifying trichilemmal cyst in a young female patient: a case report and literature review
- PMID: 37397402
- PMCID: PMC10312109
- DOI: 10.4081/dr.2022.9569
A rare ossifying trichilemmal cyst in a young female patient: a case report and literature review
Abstract
Trichilemmal cysts (TCs) constitute the second most common cutaneous cysts and are mostly presented on the scalp of middleaged women. Therefore, it is unusual for a young person to have a TC and it is extremely rare for a TC to be ossified. In the literature, only 8 cases of TCs with concomitant ossification have been described. We report the case of a 22-year-old female who presented with a scalp nodule and was treated via surgical excision of the lesion. The pathology examination of the surgical specimen revealed a lesion consisting of a multilayered squamous epithelium of slightly eosinophilic maturing keratinocytes. There was no granular layer, whereas the core of the lesion was occupied by mature bone tissue with calcium deposits. The definite diagnosis of the pathology report was ossifying TC. The aim of this report is, to enlighten clinicians about this rare pathological entity.
Keywords: ossification; recurrence; surgical excision; trichilemmal cyst.
©Copyright: the Author(s).
Conflict of interest statement
Conflict of interest: the authors declare no potential conflict of interest.
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References
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- Pusiol T, Morichetti D, Zorzi MG, Francesco P. Ossifying trichilemmal cyst. Am J Dermatopathol 2011;33:867-8. - PubMed
-
- Kamyab K, Kianfar N, Dasdar S, et al. . Cutaneous cysts: a clinicopathologic analysis of 2,438 cases. Int J Dermatol 2020;59:457-62. - PubMed
-
- Hörer S, Marrakchi S, Radner FP, et al. . A monoallelic two-hit mechanism in PLCD1 explains the genetic pathogenesis of hereditary trichilemmal cyst formation. J Invest Dermatol 2019;139:2154-63. - PubMed
-
- Baldovini C, Rosini F, Marucci G. Osseous metaplasia and mature bone formation with extramedullary hematopoiesis in trichilemmal cyst. Am J Dermatopathol 2014;36:444-6. - PubMed
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