A case of trichogerminoma: a rare cutaneous follicular neoplasm.


Journal

Pathologica
ISSN: 1591-951X
Titre abrégé: Pathologica
Pays: Italy
ID NLM: 0401123

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 30 04 2020
accepted: 18 05 2020
entrez: 2 1 2022
pubmed: 3 1 2022
medline: 5 1 2022
Statut: ppublish

Résumé

Trichogerminoma, first described by Sau et al. in 1992, is a rare cutaneous adnexal neoplasm of the hair germ cell and usually associated with benign clinical course and favorable outcome. About 30 cases have been reported, all with similar histological features. However, due to a small but potential risk of malignancy, complete excision of the tumor is the treatment of choice. There is still controversy over its inclusion into the spectrum of trichoblastoma. Herein, we report an additional case occurring in the left buttock of a 47-year-old female, presenting with a subcutaneous solitary nodule composed of lobules of basaloid cells, with peripheral palisading and round cell nests or "cell balls" arranged in the central part. The lobules are separated by a fibrous or myxoid stroma. There are no clefts separating the tumor cells and surrounding stroma, but clefts separating stroma by the surrounding adipose tissue can be seen. Typical mitotic figures are frequently present (4-5 per 10 high-power fields). Immunohistochemistry shows the tumor cells are positive for pan-CK (AE1/AE3), CK5/6, p40, GATA 3, whereas they are negative for CK7, CK20, chromogranin A, synaptofisin, androgen receptor, estrogen receptor, and calretinin. Staining for CK20, synaptofisin, and chromogranin A detect Merkel cells scattered within the lobules. Ki67 highlights a nuclear proliferative rate of about 20%. Trichogerminoma should be distinguished from other trichogenic tumors made up of basoloid cells or hair follicular differentiation. The mainly differential diagnosis includes trichoblastoma, trichoepitelioma, tricholemmoma, and basal cell carcinoma. Herein, we report a case of trichogerminoma which, unlike the cases previously reported, showed numerous mitotic figures and a higher Ki67 nuclear proliferative rate.

Identifiants

pubmed: 34974551
doi: 10.32074/1591-951X-137
pmc: PMC8720394
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

449-455

Informations de copyright

Copyright © 2021 Società Italiana di Anatomia Patologica e Citopatologia Diagnostica, Divisione Italiana della International Academy of Pathology.

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Auteurs

Marco Ungari (M)

Department of Pathology, ASST Cremona, Italy.

Giulia Tanzi (G)

Department of Pathology, ASST Cremona, Italy.

Elena Varotti (E)

Department of Pathology, ASST Cremona, Italy.

Monica Trombatore (M)

Department of Pathology, ASST Cremona, Italy.

Giuseppina Ferrero (G)

Department of Pathology, ASST Cremona, Italy.

Marino Daniel Gusolfino (MD)

Department of Pathology, ASST Cremona, Italy.

Laura Manotti (L)

Department of Pathology, ASST Cremona, Italy.

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Classifications MeSH