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Syringocystadenoma papilliferum information


Syringocystadenoma papilliferum
Other namesSyringadenoma papilliferum, Fistulous vegetative verrucous hydradenoma, Naevus syringocystadenomatosus papilliferus, Papillary syringocystadenoma, and SCAP.
An example of a syringocystadenoma papilliferum
SpecialtyDermatology
Usual onsetChildhood, Neonatal, Infancy, Adolescent.[1]
CausesGenetic.[2]
Diagnostic methodSkin biopsy.[3]
Differential diagnosisHidradenoma papilliferum, Papillary eccrine adenoma, Warty dyskeratoma, Tubular apocrine adenoma, Syringocystadenocarcinoma papilliferum.[3]
TreatmentSurgical excision.[3]

Syringocystadenoma papilliferum is a rare non-malignant adnexal neoplasm that develops from apocrine or eccrine sweat glands and can be identified histologically by cystic, papillary, and ductal invaginations into the dermis lined by double-layered outer cuboidal and luminal high columnar epithelium and connected to the epidermis.[1]

Lesions have a heterogeneous, non-distinctive appearance that ranges from skin-colored to pink-colored papules or plaques. Typically, lesions form in the head and neck area.[1]

Syringocystadenoma papilliferum can develop de-novo or within a nevus sebaceous.[4] Syringocystadenoma papilliferum tends to be seen in children. It is present at birth in approximately 50% of individuals affected, and it develops before puberty in the remaining 15%-30%.[4]

  1. ^ a b c "Syringocystadenoma papilliferum". Orphanet. Retrieved 5 October 2023.
  2. ^ "Syringocystadenoma papilliferum — About the Disease — Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2023-10-05.
  3. ^ a b c "Syringocystadenoma papilliferum". Pathology Outlines. March 10, 2022. Retrieved October 5, 2023.
  4. ^ a b Sangma, Mima Maychet B. (2013). "Syringocystadenoma Papilliferum of the Scalp in an Adult Male – A Case Report". Journal of Clinical and Diagnostic Research. 7 (4): 742–743. doi:10.7860/jcdr/2013/5452.2900. ISSN 2249-782X. PMC 3644463. PMID 23730665.

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