Atypical TDP‐43 proteinopathy clinically presenting with progressive nonfluent aphasia: A case report

• Published in: Neuropathology 2024-04, Vol.44 (2), p.154-160
• Main Authors: Suzuki, Yuki, Adachi, Tadashi, Yoshida, Kentaro, Taneda, Kenta, Sakuwa, Mayuko, Hasegawa, Masato, Hanajima, Ritsuko
• Format: Article
• Language: English
• Subjects: Amygdala; Aphasia; Atrophy; Autopsies; Autopsy; Axons; Cortex (frontal); Cortex (temporal); DNA-Binding Proteins - metabolism; Dysphagia; Frontotemporal Dementia; frontotemporal lobar degeneration; Frontotemporal Lobar Degeneration - pathology; Humans; immunoblotting; Inclusion bodies; Male; Middle Aged; Neurodegeneration; neuropathology; Phenotypes; phosphorylated transactive response DNA binding protein of 43 kDa (p‐TDP‐43); Primary Progressive Nonfluent Aphasia - pathology; progressive nonfluent aphagia; Putamen; Tau protein; TDP-43 Proteinopathies - pathology
• ISSN: 0919-6544; 1440-1789
• DOI: 10.1111/neup.12942

Progressive nonfluent aphasia (PNFA) is a form of frontotemporal lobar degeneration (FTLD) caused by tau and transactive response DNA‐binding protein of 43 kDa (TDP‐43) accumulation. Here we report the autopsy findings of a 64‐year‐old right‐handed man with an atypical TDP‐43 proteinopathy who presented with difficulties with speech, verbal paraphasia, and dysphagia that progressed over the 36 months prior to his death. He did not show pyramidal tract signs until his death. At autopsy, macroscopic brain examination revealed atrophy of the left dominant precentral, superior, and middle frontal gyri and discoloration of the putamen. Spongiform change and neuronal loss were severe on the cortical surfaces of the precentral, superior frontal, and middle frontal gyri and the temporal tip. Immunostaining with anti‐phosphorylated TDP‐43 revealed neuronal cytoplasmic inclusions and long and short dystrophic neurites in the frontal cortex, predominantly in layers II, V, and VI of the temporal tip, amygdala, and transentorhinal cortex. Immunoblot analysis of the sarkosyl‐insoluble fractions showed hyperphosphorylated TDP‐43 bands at 45 kDa and phosphorylated C‐terminal fragments at approximately 25 kDa. The pathological distribution and immunoblot band pattern differ from the major TDP‐43 subtype and therefore may represent a new FTLD‐TDP phenotype.