Abstract

Poroid hidradenoma (PH) is a rare, benign adnexal neoplasm usually presenting as a solitary, well circumscribed, asymptomatic papule or nodule that appears reddish and is occasionally tender. Since 1990, only a few cases of PH have been reported. We present a case of PH on the medial surface of the thigh and describe, for the first time, the dermoscopic and reflectance confocal microscopic (RCM) features in correlation with histology. A 67-year-old woman with unremarkable family or past medical history presented with a nodular lesion on the medial surface of the right thigh. The lesion had appeared 4 months earlier and rapidly enlarged. Physical examination revealed a 7 × 5 mm, non-tender, reddish nodule with clinically distinct margins. Dermoscopy showed central blue-grey pigmented areas, a polymorphous vascular pattern with arborizing, glomerular and hairpin vessels surrounded by white halos. RCM revealed an ovoid, well-outlined tumor, with a central area containing cells with distinctive morphologies, two types of tumor cells, tubular hypo-reflective structures, and rectilinear vessels in the stroma. These findings correlated with histological features, which established the diagnosis of PH. Even though the diagnosis of PH remains histopathological, non-invasive tools, such as RCM, can help rule out several malignancies, therefore reducing surgical-associated comorbidity.

Highlights

  • Poroid hidradenoma (PH), a benign neoplasm with eccrine differentiation, was originally described by Abenoza and Ackerman in 1990 [1]

  • We report a case of PH with dermoscopic and reflectance confocal microscopy (RCM) findings, in correlation with histology

  • The differential diagnosis included basal cell carcinoma, an adnexal, pyogenic granuloma, malighalos (Figure 1C). nant eccrine poroma [6], and melanoma

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Summary

Introduction

Poroid hidradenoma (PH), a benign neoplasm with eccrine differentiation, was originally described by Abenoza and Ackerman in 1990 [1]. Only a few cases have been reported in the literature [2]. PH is wholly intra-dermal, only rarely merging with the epidermis, and shows architectural features of hidradenoma and cytologic features of poroid neoplasms. PH rarely becomes malignant, the treatment consists of the complete surgical excision of the lesion in order to prevent recurrence [5]. PH has been histologically well defined, its dermoscopic features are rarely reported and there is no available confocal description of this tumor. We report a case of PH with dermoscopic and reflectance confocal microscopy (RCM) findings, in correlation with histology.

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