“Madura Head”—A Rare Case of Craniocerebral Maduromycosis

Author:

Behera Bikash1,Mishra Sanjib1,Dhir Manmath1,Panda Rabi1,Samantaray Sagarika2

Affiliation:

1. Department of Neurosurgery, SCB Medical College, Cuttack, Odisha, India

2. Department of Pathology, AHRCC, Cuttack, Odisha, India

Abstract

AbstractAs maduromycosis is mostly confined to lower extremities. It was rightly named as “Madura foot” by John Gill in 1842, after the name of Madurai district, in Tamil Nadu state of India. Mycetoma is a chronic granulomatous infection mostly caused by a true fungus, Madurella mycetomatis (Eumycotic mycetoma). Craniocerebral involvement by eumycotic mycetoma is rare in world literature and confined to few case reports only. Here we present an interesting case of craniocerebral maduromycosis presenting with focal seizure, hemiparesis, and multiple discharging sinuses all over the scalp. The patient was diagnosed by histopathologic biopsy and managed conservatively with antifungal medications in view of widespread involvement of the scalp, not amenable to surgery.

Publisher

Georg Thieme Verlag KG

Subject

Materials Chemistry

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Craniocerebral Maduramycosis: Masquerading as a Tumor;Asian Journal of Neurosurgery;2022-12

2. Cranial mycetoma: A rare case report with review of literature;Journal of Global Infectious Diseases;2021

3. Invasive Fungal Infections of the Central Nervous System in Immune-Competent Hosts;Current Fungal Infection Reports;2020-04-11

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