A Misdiagnosed Familiar Brooke-Spiegler Syndrome: Case Report and Review of the Literature.

Brooke–Spiegler syndrome adnexal neoplasm cylindroma eccrine cylindromatosis neurofibromatosis type 1 spiradenocylindroma spiradenoma trichoepithelioma

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
12 Apr 2024
Historique:
received: 04 03 2024
revised: 21 03 2024
accepted: 08 04 2024
medline: 27 4 2024
pubmed: 27 4 2024
entrez: 27 4 2024
Statut: epublish

Résumé

Aim of the report: Brooke-Spiegler syndrome (BSS) is a rare autosomal dominant disease characterized by the growth of cylindromas, spiradenomas, trichoepitheliomas, or their combination. These neoplasms usually begin in the second decade and progressively increase in number and size over the years. Diagnosis necessitates consideration of family history, clinical examination, histological findings, and genetic analysis. The aim of this paper is to explore the clinical overlap between Brooke-Spiegler syndrome (BSS) and neurofibromatosis type 1 (NF1). We aim to highlight the challenges associated with their differential diagnosis and emphasize the lack of standardized diagnostic criteria and treatment approaches. Case presentation: Hereby, we introduce the case of a 28-year-old male referred for suspicion of neurofibromatosis type 1 (NF1) who initially declined the recommended surgical excision for a scalp mass. After four years, he returned with larger masses of the scalp, and underwent excision of multiple masses, revealing cylindromas, spiradenomas, and spiradenocylindromas. Family history reported similar tumors in his father, who was also diagnosed with NF1 for the presence of multiple subcutaneous lesions on the scalp. Clinical overlap led to a genetic consultation, but testing for CYLD mutations yielded no significant variations. Despite this, the strong family history and consistent findings led to a revised diagnosis of Brooke-Spiegler syndrome, correcting the initial misdiagnosis of NF1 syndrome. Conclusions: Thanks to the evolving landscape of BSS research over the past two decades, its molecular underpinnings, clinical presentation, and histopathological features are now clearer. However, a thorough family history assessment is mandatory when BSS is suspected. It is our belief that a multidisciplinary approach and cooperation between specialists are essential when dealing with BSS. By sharing this case, we hope to underscore the importance of considering BSS as a differential diagnosis, especially in cases with atypical presentations or overlapping features with other syndromes like NF1.

Identifiants

pubmed: 38673513
pii: jcm13082240
doi: 10.3390/jcm13082240
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Auteurs

Tito Brambullo (T)

Clinic of Plastic Surgery, Neurosciences Department, University of Padua, 35131 Padua, Italy.

Alberto De Lazzari (A)

Clinic of Plastic Surgery, Neurosciences Department, University of Padua, 35131 Padua, Italy.

Arianna Franchi (A)

Clinic of Plastic Surgery, Neurosciences Department, University of Padua, 35131 Padua, Italy.

Eva Trevisson (E)

Clinical Genetics Unit, Department of Women and Children's Health, University of Padova, 35131 Padua, Italy.

Maria Luisa Garau (ML)

Clinical Genetics Unit, Department of Women and Children's Health, University of Padova, 35131 Padua, Italy.

Federico Scarmozzino (F)

Surgical Pathology & Cytopathology Unit, Department of Medicine (DIMED), University of Padova, 35131 Padova, Italy.

Vincenzo Vindigni (V)

Clinic of Plastic Surgery, Neurosciences Department, University of Padua, 35131 Padua, Italy.

Franco Bassetto (F)

Clinic of Plastic Surgery, Neurosciences Department, University of Padua, 35131 Padua, Italy.

Classifications MeSH