Postautologous Hematopoietic Stem Cell Transplantation Disseminated Hypopigmented Keratosis

Disseminated hypopigmented keratosis is a rare distinct clinical entity. This report describes the case of a 19-year-old male patient who developed disseminated hypopigmented keratosis 2 months after autologous hematopoietic stem cell transplantation for pineal choriocarcinoma. The patient displayed numerous tiny whitish or depigmented macules and papules on the chest, back, posterior neck, shoulders, arms, and thighs, closely resembling lichen nitidus. Microscopically, the lesion was orthokeratotic, acanthotic, and flat-bottomed without cytological atypia. Dermal inflammation was minimal. Fontana-Masson, Melan-A, and sex-determining region Y-box transcription factor 10 staining revealed a significant decrease in both basal melanin content and the number of melanocytes. The patient was initially administered a topical agent comprising hydrocortisone and urea, which exhibited minimal improvement. This case report suggests that disseminated hypopigmented keratosis may be a rare cutaneous manifestation of autologous hematopoietic stem cell transplantation. Additional research is necessary to gain a more comprehensive understanding of the pathogenesis and the clinical course of this disease.

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Publication Details

Journal
American Journal of Dermatopathology
Published
2024-12-10
DOI
https://doi.org/10.1097/dad.0000000000002895
Primary Topic
melanin and skin pigmentation
Type
article
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article

Postautologous Hematopoietic Stem Cell Transplantation Disseminated Hypopigmented Keratosis

Supasan Sripodok, Nan‐Lin Wu, Yu‐Hung Wu
American Journal of Dermatopathology
melanin and skin pigmentation
article

Postautologous Hematopoietic Stem Cell Transplantation Disseminated Hypopigmented Keratosis

Supasan Sripodok, Nan‐Lin Wu, Yu‐Hung Wu
article en

Abstract

Disseminated hypopigmented keratosis is a rare distinct clinical entity. This report describes the case of a 19-year-old male patient who developed disseminated hypopigmented keratosis 2 months after autologous hematopoietic stem cell transplantation for pineal choriocarcinoma. The patient displayed numerous tiny whitish or depigmented macules and papules on the chest, back, posterior neck, shoulders, arms, and thighs, closely resembling lichen nitidus. Microscopically, the lesion was orthokeratotic, acanthotic, and flat-bottomed without cytological atypia. Dermal inflammation was minimal. Fontana-Masson, Melan-A, and sex-determining region Y-box transcription factor 10 staining revealed a significant decrease in both basal melanin content and the number of melanocytes. The patient was initially administered a topical agent comprising hydrocortisone and urea, which exhibited minimal improvement. This case report suggests that disseminated hypopigmented keratosis may be a rare cutaneous manifestation of autologous hematopoietic stem cell transplantation. Additional research is necessary to gain a more comprehensive understanding of the pathogenesis and the clinical course of this disease.

American Journal of DermatopathologyVol. 47(2)
Siriraj Hospital (TH), Mahidol University (TH), Mackay Memorial Hospital (TW), Mackay Medical University (TW)
Openalex Percentile: Top 76%
melanin and skin pigmentation
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Postautologous Hematopoietic Stem Cell Transplantation Disseminated Hypopigmented Keratosis — Supasan Sripodok, Nan‐Lin Wu, et al. · American Journal of Dermatopathology (2024) | TGRS Research Map | TGRS