Syringocystadenoma papilliferum
| Syringocystadenoma papilliferum | |
|---|---|
| Other names | Syringadenoma papilliferum, Fistulous vegetative verrucous hydradenoma, Naevus syringocystadenomatosus papilliferus, Papillary syringocystadenoma, and SCAP. |
Surgical excision.[3] | |
Syringocystadenoma papilliferum is a rare non-malignant adnexal neoplasm that develops from
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]
Symptoms and Signs
Symptoms of Syringocystadenoma papilliferum include papules, lack of hair on the scalp, blisters, subcutaneous nodules, and nevus sebaceous.[2]
Diagnosis
A skin biopsy is used to diagnose syringocystadenoma papilliferum. Characteristics of Syringocystadenoma papilliferum are dilated capillaries and a dense infiltration of plasma cells.[1]
Differential diagnoses include papillary eccrine adenoma, warty dyskeratoma, tubular apocrine adenoma, and hidradenoma papilliferum.[3]
See also
- List of cutaneous conditions
- Hidradenoma papilliferum
- Papillary eccrine adenoma
- List of cutaneous conditions associated with increased risk of nonmelanoma skin cancer
References
- ^ a b c d "Syringocystadenoma papilliferum". Orphanet. Retrieved 5 October 2023.
- ^ a b c "Syringocystadenoma papilliferum — About the Disease — Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2023-10-05.
- ^ a b c d "Syringocystadenoma papilliferum". Pathology Outlines. March 10, 2022. Retrieved October 5, 2023.
- ^ PMID 23730665.