Cutaneous Findings of Sporadic, Adult-Onset Neuronal Intranuclear Inclusion Disease. (19th January 2022)

• Record Type: Journal Article
• Authors: Moran, Jakob M. T.; Eikermann-Haerter, Katharina; Rapalino, Otto; Dang, Timothy M.; Holmes, Robert K.; Chen, Steven T.; Hoang, Mai P.
• Is Part Of: American journal of dermatopathology. Volume 44:Number 1(2022)
• Page Start: 1
• Page End: 6
• Publication Date: 2022-01-19
• Subjects: neuronal -- intranuclear -- inclusion -- ubiquitin -- electron microscopy; Skin -- Diseases -- Periodicals; Histology, Pathological -- Periodicals; 616.50705
• DOI: 10.1097/DAD.0000000000001955
• Languages: English
• ISSNs: 0193-1091

Abstract

Abstract: Neuronal intranuclear inclusion disease is a rare, progressive neurodegenerative disease whose hallmark histopathologic finding is the presence of ubiquitin-positive hyaline intranuclear inclusions in neuronal and non-neuronal cells. We present a case of neuronal intranuclear inclusion disease in a 61-year-old Asian man with a history of repeated episodes of altered mental status, long-standing bladder dysfunction, and cerebrovascular accidents. The patient had characteristic magnetic imaging findings of high signal along the cortico–medullary junction on diffusion-weighted sequences and symmetric T2 hyperintensity in the paravermal area of the cerebellum. Skin biopsies showed characteristic histopathologic findings of ubiquitin-positive intranuclear inclusions that ultrastructurally composed of filamentous material without limiting membrane within eccrine epithelium and dermal fibroblasts. Our case highlights the utility of readily accessible skin biopsy in the diagnosis of this rare neurodegenerative disease.