Clinicopathologic and genetic features of multiple system atrophy with Lewy body disease.
Shunsuke KogaFuyao LiNa ZhaoShanu F RoemerTanis J FermanAnna I WernickRonald L WaltonAyman H FaroqiNeill R Graff-RadfordWilliam P CheshireOwen A RossGourisankar GhoshPublished in: Brain pathology (Zurich, Switzerland) (2020)
Although rare, MSA with transitional or diffuse LBD can develop clinical features of PDD or DLB. Minimal change MSA can be interpreted as a coincidental, but distinct, α-synucleinopathy in a subset of patients with diffuse LBD.