Grover’s Disease Association with Cutaneous Keratinocyte Cancers: More than a Coincidence?

Author:

Nedelcu Roxana12,Dobre Alexandra13ORCID,Turcu Gabriela124ORCID,Andrei Razvan45,Balasescu Elena1ORCID,Pantelimon Florentina2,David-Niculescu Mihaela26,Dobritoiu Adina2,Radu Raluca7,Zaharia Georgiana Roxana7,Hulea Ionela1,Brinzea Alice128,Manea Lorena9,Gherghiceanu Mihaela1011,Ion Daniela1

Affiliation:

1. Pathophysiology Department, “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania

2. Derma360 Clinic, 011273 Bucharest, Romania

3. Oncologic Dermatology Department, Elias Emergency University Hospital, 011461 Bucharest, Romania

4. Dermatology Department, Colentina Clinical Hospital, 020125 Bucharest, Romania

5. Synevo, 014192 Bucharest, Romania

6. Dermatology Department, “Grigore Alexandrescu” Emergency Pediatric Hospital, 011743 Bucharest, Romania

7. Dermatology Department, Central Military Emergency Hospital “Dr.Carol Davila”, 010242 Bucharest, Romania

8. National Institute for Infectious Diseases “Prof. Dr. Matei Balș”, 021105 Bucharest, Romania

9. Dermatology Department, Pitié-Salpêtrière University Hospital, Public Assistance—Paris Hosiptals—AP-HP—Charles Foix, 75013 Paris, France

10. Cellular, Molecular Biology & Histology Department, “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania

11. Ultrastructural Pathology and Bioimaging Lab, Victor Babeş National Institute of Pathology, 050096 Bucharest, Romania

Abstract

Better mechanistic understanding of desmosome disruption and acantholysis in Grover’s disease (GD) may improve management of this disease. Recent molecular studies highlighted promising pathways to be explored by directly comparing GD and selected features of associated skin diseases. The association between GD and cutaneous keratinocyte carcinomas, the most prevalent non-melanoma skin cancers (NMSC), is not completely characterized. To review the medical literature regarding GD-associated cutaneous keratinocyte cancers, focusing on molecular features, pathophysiological mechanisms, and disease associations, to help guide future research and patient management. GD has been associated with a variety of skin conditions, but its association with skin cancers has been rarely reported. Between 1983 and 2024, only nine scientific papers presented data supporting this association. Interestingly, we found that GD may mimic multiple NMSCs, as few authors reported GD cases misdiagnosed as multiple cutaneous squamous cell carcinomas for more than 4 years or the presence of superficial basal cell carcinoma-like areas associated with focal acantholysis. In conclusion: (a) GD may be an imitator of multiple NMSCs, and (b) the relationship between GD and NMSCs may reveal promising pathways for the mechanistic understanding of desmosome disruption and acantholysis in GD and may even lead to its reclassification as a distinctive syndrome.

Funder

University of Medicine and Pharmacy Carol Davila

Publisher

MDPI AG

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