|Yasunobu Kato, Toshiyuki Yamamoto*|
|Corresponding Author: Prof. Toshiyuki Yamamoto, MD, PhD, Department of Dermatology, Fukushima Medical University, Hikarigaoka 1, Fukushima 960-1295, Japan. Tel./Fax: +81.24.547.1307 E-mail: firstname.lastname@example.org|
|Received: July 7, 2015; Accepted: August 3, 2015; Published: August 29, 2015;|
|Citation: Kato Y, Yamamoto T (2015) Infantile perianal pyramidal protrusion. Dermatol Clin Res, 1(2): 39-40.|
|Copyrights: ©2015 Kato Y, Yamamoto T. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.|
TO THE EDITOR,
A 10-month-old, otherwise healthy girl visited Hanawa Kosei Hospital, presenting with a nodule in the perianal area. Her mother noticed it three weeks previously. Physical examination revealed a well-circumscribed, solitary, smooth-surface, reddish protruded nodule located anterior to the anus (Fig. 1). Her mother did not wish examination by biopsy. She is now under observation, but currently without marked changes.
Infantile perianal pyramidal protrusion was first described by Kayashima et al. , which appears at birth or soon. To date, nearly 100 cases have been reported , and almost all of the reported patients are girl. The diagnosis is usually made based on its characteristic clinical features, which are not only pyramidal, but also expressed as “peanut”, “hen’s crest”, “leaf like”, or “tongue tip”. Also, parents often do not wish biopsy or surgical intervention.
Infantile perianal pyramidal protrusion is classified into constitutional, functional, and lichen sclerosus-associated type. Additionally, Verma and Wollina  reported a case of infantile perianal pyramidal protrusion with an adjacent hemangiomatous plaque, raising a possibility that infantile perianal pyramidal protrusion may be a part of incomplete PELVIS (perineal hemangioma, external genitalia malformations, lipomyelomeningocoele, vesicorenal abnormalities, imperforate anus, and skin tag) syndrome. Histology reveals elongated epidermis, dermal edema and fibrosis, with dilated vessels and mild cellular infiltrates. Lichen sclerosus-like changes can be seen in a subgroup.
Although the etiology of infantile perianal pyramidal protrusion is
still unclear, an anatomic weakness in the perineum may be associated. Whether
infantile perianal pyramidal protrusion resolves spontaneously or not is still
controversial, which may depend on the above three types. Constitutive type is suggested to remain
unchanged for many years. Functional type is associated with dietary changes,
diarrhea, and constipation, and can be much improved by dietary modification. Lichen
sclerosus-type is expected to respond to topical corticosteroid therapy
. Our case is planned to be under
long-term conservative follow-up.
1. Kayashima K-I, Kitoh M, Ono T. Infantile perianal pyramidal protrusion. Arch Dermatol 1996; 132: 1481-1484.
2. Zavras N, Christianakis E, Tsamoudaki S, Velaoras K. Infantile perianal pyramidal protrusion: a report of 8 new cases and a review of the literature. Case Rep Dermatol 2012; 4: 202-206.
3. Verma SB, Wollina U. Infantile perianal pyramidal protrusion with coexisting perineal and perianal hemangiomas: a fortuitous association or incomplete PELVIS syndrome? Indian J Dermatol 2014; 59: 71-74.
4. Kim BJ, Woo SM, Li K, Lee DH, Cho S. Infantile perianal pyramidal protrusion treated by topical steroid application. J Eur Acad Dermatol Venereol 2007; 21: 263-264.
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