| Literature DB >> 30684817 |
Joo Yeon Kim1, Ji Yeon Kim1, Myungchan Park2, Cheol Kyu Oh2, Jae-Seung Chung2, Sang Hyun Park2, Seong Cheol Kim3.
Abstract
INTRODUCTION: Pseudoepitheliomatous keratotic and micaceous balanitis (PKMB) is an extremely rare disease. Herein, we report a case of PKMB in a patient who underwent two surgical procedures, since the 5-FU cream was not available. PRESENTATION OF CASE: A 50 year-old Korean man undergoing circumcision in a local clinic presented with a tumor-like lesion on the glans penis. Peeling the mass was performed to remove the entire mass after an excisional biopsy. A pathologic finding of mass showed hyperkeratotic and papillomatous squamous epithelium without obvious cytologic atypia. Considering that the lesion recurred after 4 weeks, the patient underwent glansectomy with split-thickness skin graft (STSG). There had been no evidence of recurrence at the surgical site during the follow-up at 6 years postoperatively. DISCUSSION: If the 5-FU cream is not available, two surgical procedures can be performed for treatment and biopsy. Peeling the mass has the advantage of confirming the characteristics of the whole lesion, but it cannot confirm tumor invasion because it is unable to obtain the subepithelial layer. Glansectomy is able to accurately identify the tumor stage because it removes the tumor and total glans penis and has excellent outcome.Entities:
Keywords: Balanitis; Penile neoplasms; Penis; Treatment outcome; Urologic surgical procedures
Year: 2019 PMID: 30684817 PMCID: PMC6351345 DOI: 10.1016/j.ijscr.2018.12.008
Source DB: PubMed Journal: Int J Surg Case Rep ISSN: 2210-2612
Fig. 1Pseudoepitheliomatous keratotic and micaceous balanitis (PKMB).
(a) Mica-like crusts and hard keratotic mass found in almost the entire glans penis. (b) A hyperkeratotic plaque is easily separated from the glans penis. (c) After the complete removal of the hard mass, oozing blood is observed on the separated surface.
Fig. 2(a) Hyperkeratotic and papillomatous squamous epithelium with broad pushing margin. Subepithelial stromal tissue not obtained in this specimen (×12.5). (b) On high power view (×100), it is characterized by papillomatosis with fibrovascular cores. Keratinocytes show clear cytoplasm and winkled nuclei, also called as “koilocytosis,” which is consistent with HPV-related cytopathic changes, but not obvious cytologic atypia.
Fig. 4(a) There are condylomatous and rounded arborescent papillae with prominent fibrovascular cores. The superficial portion of the squamous epithelium shows well-differentiated and koilocytotic atypia (×12.5). (b) At the invasive margin in the deeper portion, the tumor-stromal interface is irregular and destructive, which is not seen in a giant condyloma. Malignant cells show enlarged nuclei with an irregular configuration, and occasionally dyskeratotic cells are noted (×100).
Fig. 5Final follow-up findings at 6 years after surgery.