Abstract
Syringocystadenoma papilliferum (SCAP) is a rare benign skin adnexal tumour commonly (50%) found in infants and children and less commonly (15–30 %) found at puberty and in adolescents. It usually presents as irregular papule or smooth hairless plaque on the scalp and forehead, however, nodular or verrucous transformation is reported at puberty. Microscopically it is characterized by ducts connecting to the surface, containing papillary processes and lined with two epithelial layers. Head and neck is the commonest (75%) and lower extremity is the rarest reported location. Here we report a case series of SCAP at five different locations throughout the body. The clinical and histological features and the differential diagnoses are also discussed.
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Katoulis AC, Bozi E. Syringocystadenoma papilliferum. Orphanet Encyclopedia. 2004
Pinkus H. Life history of naevus syringocystadenomatous papilliferus. Arch Dermatol Syphil 1954; 69:305–322
Helwig EB, Hackney VC. Syringoadenoma papilliferum. Arch Dermatol 1995; 71:361–372
Mammino JJ, Vidmar DA. Syringocystadenoma papilliferum. Int J Dermatol 1991; 30:763–766
Bondi R, Urso C. Syringocystadenoma papilliferum. Histopathology 1996; 28:475–477
Premlatha S, Rao NR, et al. Segmental syringocystadenoma papilliferum in an unusual location. Int J Dermatol 1985; 24:520–521
Koga T, Kubota Y, Nakayama J. Syringocystadenoma papilliferum without an antecedent naevus sebaceous. Acta Derm Venereol 1999; 79:237
Patterson JW, Straka BF, Wick MR. Linear syringocystadenoma papilliferum of the thigh. J Am Acad Dermatol 2001; 45:139–141
Karg E, Korom L, Varga E, Ban G, Turi S. Congenital syringocystadenoma papilliferum. Pediatr Dermatol 2008; 25:132–133
Rammeh-Rommani S1, Fezaa B, Chelbi E, Kammoun MR, Ben Jilani SB, Zermani R. Syringocystadenoma papilliferum: report of 8 cases. Pathologica 2006; 98:178–180
Townsend TC, Bowen AR, Nobuhara KK. Syringocystadenoma papilliferum: an unusual cutaneous lesion in a pediatric patient. J Pediatr 2004; 145:131–133
Askar S, Kiline N, Aytekin S. Syringocystadenoma papilliferum mimicking basal cell carcinoma on the lower eyelid: a case report. Acta Chir Plast 2002; 44:117–119
Suzuki T, Ikeda H, Hamasaki Y, Hatamochi S, Yamazaki S. Syringocystadenoma papilliferum associated with apocrine poroma. J Dermatol 2006; 33:249–251
Yamamoto O, Doi Y, Hamada T, Hisaoka M, Sasaguri Y. An immunohistochemical and ultrastructural study of Syringocystadenoma papilliferum. Dermatol Online J 2003; 9:7
Niizuma K. Syringocystadenoma papilliferum: light and electron microscopic studies. Acta Derm Venerol 1976; 56:327–336
Chi CC, Tsai RY, Wang SH. Syringocystadenoma papilliferum: successfully treated with Moh’s micrographic surgery. Dermatol Surg 2004; 30:468–471
Kumar V, Garg RB, Baruah CM, Ratnakar C. Syringocystadenoma papilliferum. Indian J Dermatol Venereol Leprol 1991; 57:150–151
Golvalkar RM, Rashed G. Syringocystadenoma papilliferum arising in a naevus sebaceous. Indian J Dermatol Venereol Leprol 1994; 60:340–342
Sood A, Khanna N, Kumar R. Syringocystadenoma papilliferum at unusual sites. Indian J Dermatol Venereol Leprol 2000; 66:328–329
Malhotra P, Singh A, Ramesh V. Syringocystadenoma papilliferum on the thigh: an unusual location. Indian J Dermatol Venereol Leprol 2009; 75:170–172
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Basu, A., Dutta, M.K., Maiti, S. et al. Syringocystadenoma papilliferum: A case series and review of the literature in Indian context. Hellenic J Surg 86, 98–101 (2014). https://doi.org/10.1007/s13126-014-0105-1
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DOI: https://doi.org/10.1007/s13126-014-0105-1