Increased number of mitochondria in capillaries distributed in stroke‐like lesions of two patients with MELAS

• Published in: Neuropathology Vol. 39; no. 5; pp. 404 - 410
• Main Authors: Yamadera, Misaki, Fujimura, Harutoshi, Shimizu, Yuri, Matsui, Misa, Nakamichi, Itsuko, Yokoe, Masaru, Sakoda, Saburo
• Format: Journal Article
• Language: English
• Published: Melbourne John Wiley & Sons Australia, Ltd 01.10.2019; Wiley Subscription Services, Inc
• Subjects: Acidosis; Adult; and stroke‐like episodes; Arterioles; Astrocytes; Atrophy; Autopsy; Brain - pathology; Capillaries; Capillaries - pathology; Cerebellum; Cerebrum; Encephalopathy; Endothelial cells; Endothelial Cells - pathology; Female; Humans; Immunoreactivity; Lactic acidosis; lacticacidosis; Lesions; Male; MELAS syndrome; MELAS Syndrome - complications; MELAS Syndrome - pathology; Middle Aged; Mitochondria; Mitochondria - pathology; mitochondrial angiopathy; mitochondrial myopathy; Myopathy; Pial artery; Smooth muscle; Stroke; Stroke - etiology; Stroke - pathology; stroke‐like lesion; Territory; Translocase; and stroke-like episodes; mitochondrial myopathy; capillaries; lacticacidosis; mitochondria; stroke-like lesion; mitochondrial angiopathy; encephalopathy
• ISSN: 0919-6544; 1440-1789
• DOI: 10.1111/neup.12593

We investigated two autopsy cases of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS) using immunohistochemical staining with an anti‐mitochondrial antibody against translocase of the outer membrane 20 (TOMM20). In case 1, the patient was a 42‐year‐old man with a disease duration of 53 days, and in case 2, the patient was a 62‐year‐old woman with a disease duration of 27 months. In both the cases autopsy revealed moderate atrophy of the cerebrum and cerebellum and multifocal necrotizing lesions, irrespective of the vascular territory. Case 1 showed multiple areas with total necrosis in the cortex, accompanied by increases in number of protoplasmic astrocytes and acidophilic neurons as well as axonal swelling, suggestive of acute or subacute stage stroke‐like lesions (SLLs). In case 2, most of the SLLs displayed laminar spongy change in a rarefied cortex, and were considered to be at the chronic stage. In both the cases, capillary proliferation was noted within the SLLs, particularly in the acute phase. Endothelial cells of proliferating capillaries were strongly positive for TOMM20. In the cortex outside the SLLs, microvessels displayed only a fine granular immunoreactivity, as is seen in the controls. Although smooth muscle cells and endothelial cells in pial arteries and arterioles were also strongly positive for TOMM20, the territories of the affected pial arteries and arterioles did not correlate with the distribution of the SLLs. Although MELAS is characterized by recurrent stroke‐like episodes (SLEs), the pathogenetic relationship between SLEs and mitochondrial angiopathy remains unknown. An aberrant increase of mitochondria in the capillary endothelial cells of SLLs may disturb endothelial function, thus playing a role in the formation or development of SLLs.