Poroid Neoplasms: A Clinicopathological Study of 13 Cases

Author:

Efared Boubacar12ORCID,Boubacar Idrissa2,Ousmane Kadre Kadre Alio13,Abani Bako Aïchatou Balaraba13,Boureima Habiba Salifou3,Amadou Soumaila4,Nouhou Hassan1

Affiliation:

1. Faculty of Health Sciences, Abdou Moumouni University, Niamey, Niger

2. Pathology laboratory, Niamey National Hospital, Niamey, Niger

3. General Referral Hospital, Niamey, Niger

4. Department of surgery, Niamey National Hospital, Niamey, Niger

Abstract

Introduction: Poroid neoplasms (PN) are a heterogeneous group of tumors deriving from sweat glands and folliculo-sebaceous units. Their histological classification and clinical features are challenging. Our aim was to report clinicopathological features of poroid neoplasms. Methods: It is a retrospective study including all cases of poroid neoplasms registered at our Pathology laboratory of Niamey National Hospital (February 2020-February 2024). Results: We registered 13 cases of benign poroid neoplasms: 10 classic poromas (CP) (76.9%), 2 poroid hidradenomas (PH) (15.4%) and 1 dermal duct tumor (DDT) (7.7%). Nine cases (69.2%) had preoperative clinical diagnosis of malignancy. The mean age was 41.1 years (range of 12-70 years) with a slight female predominance. Only 4/13 cases (30.8%) had classical palmoplantar locations. The tumors mean size was 3.7 cm (range of 0.4-8 cm). Clear cells were present in 7 cases (53.8%), apocrine ductal differentiation (mixed or pure) in 6 cases (46.2%), keratin horns in 2 cases (15.4%), squamous eddies in 6 cases (46.2%), melanin pigments in 1 case (7.7%) and sebaceous differentiation in 2 cases (15.4%). Conclusions: Unlike what is classically reported, our study shows that apocrine ductal differentiation, younger age and non-palmoplantar locations are common in poroid neoplasms.

Publisher

SAGE Publications

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