Wernicke's Disease and Schizophrenia: A Case Report and Review of the Literature

1996 ◽  
Vol 26 (3) ◽  
pp. 319-328 ◽  
Author(s):  
Manuel F. Casanova

Objectives: A review of the neuropathology literature in schizophrenia suggests that some patients with this disease exhibit periventricular gliosis at postmortem examination. Several researchers have speculated that this finding is the remnant of either a prior viral infection or a gestational intraventricular hemorrhage. The present article uses a case report to hypothesize and discuss an alternate possibility to the putative gliosis, namely Wernicke's disease. Method: Based on the pathological findings of our patient and a review of the literature, the author summarizes several reasons why Wernicke's disease may occur, and still be unnoticed, in some schizophrenic patients. Results: Inefficient self-care and homelessness predisposes some patients with schizophrenia to poor dietary habits and malnutrition. Similarly, the high prevalence of concurrent alcoholism in patients with schizophrenia may propitiate thiamine deficiency. The resulting brain insult may be compounded by disturbances of carbohydrate metabolism which may be peculiar to the schizophrenic process itself, or acquired, as in coincidental diabetes. Conclusions: Since symptoms accrued to Wernicke's may often be subtle and obscured by other schizophreniform manifestations, clinicians should lower their threshold for suspecting this potentially fatal complication. The diagnostic possibility of Wernicke's should be especially entertained in schizophrenic patients who are alcoholics and/or diabetics.

2011 ◽  
Vol 28 (2) ◽  
pp. 327-330 ◽  
Author(s):  
Jason D. Hill ◽  
Michael S. Rhee ◽  
John R. Edwards ◽  
Matthew C. Hagen ◽  
Daniel H. Fulkerson

2005 ◽  
Vol 91 (1) ◽  
pp. 90-92 ◽  
Author(s):  
Roberto Buzzoni ◽  
Silvia Della Torre ◽  
Diego Cortinovis ◽  
Laura Catena

Synchronous multicentric osteosarcoma is a rare entity with fewer than 100 well documented cases in the medical literature. The disease usually progresses rapidly in young patients and slightly slower in adults. We present a case of synchronous multicentric osteosarcoma with some peculiarities in a 73-year-old woman. The diagnosis was made after postmortem examination, which underlines the importance of this procedure. This case report is accompanied by a review of the literature.


2003 ◽  
Vol 11 (3) ◽  
pp. 153-156 ◽  
Author(s):  
Mark Sheldon Lloyd ◽  
Naguib El-Muttardi ◽  
A Robson

Eccrine porocarcinoma is a rare form of skin cancer that is often con-fused with other types of skin malignancy The present paper high-lights a typical case to remind plastic surgeons of the natural history, pathological findings and current literature on the management of this cancer.


2018 ◽  
Vol 2018 ◽  
pp. 1-5
Author(s):  
Rauf Melekoglu ◽  
Ebru Celik ◽  
Hasim Kural

Intrauterine transfusion is the most common and successful intrauterine procedure for the treatment of fetal anemia due to red cell alloimmunization. Fetal intracranial hemorrhage is a very rare complication of intrauterine transfusion in patients with Rh(D) alloimmunization and it has been demonstrated only in a few case reports in the literature. Herein, we described a case of grade IV intraventricular hemorrhage that was diagnosed following the first intrauterine transfusion and reviewed the literature about the fetal intracranial hemorrhage that occurred after intrauterine intravascular transfusion procedure.


2007 ◽  
Vol 22 ◽  
pp. S139
Author(s):  
T. Sanchez-Araña Moreno ◽  
J.L. Hernandez Fleta ◽  
M.E. Terres Ruiz ◽  
J.M. Brito Jinorio ◽  
A. Salesansky Davidovsky ◽  
...  

2012 ◽  
Vol 48 (3) ◽  
pp. 174-180 ◽  
Author(s):  
Venkatesh S. Madhugiri ◽  
Sudheer Kumar Gundamaneni ◽  
Awdhesh Kumar Yadav ◽  
Gopalakrishnan M. Sasidharan ◽  
Kumar V.R. Roopesh

2017 ◽  
Vol 102 ◽  
pp. 695.e7-695.e10 ◽  
Author(s):  
Aristotelis S. Filippidis ◽  
Taylor J. Conroy ◽  
Georgios A. Maragkos ◽  
James W. Holsapple ◽  
Keith G. Davies

Neurosurgery ◽  
1985 ◽  
Vol 16 (3) ◽  
pp. 391-394 ◽  
Author(s):  
Charles E. Alpers ◽  
Michael S.B. Edwards

Abstract A striking and diffuse hemangiomatous architecture was identified by microscopic examination of bone specimens obtained at cranial synostectomy and from the craniofacial area of a young boy with Kleeblättschadel deformity and Crouzon's syndrome. A retrospective review of the histopathological appearance of bone specimens from other patients with Crouzon's syndrome treated on our service and a review of the literature on craniosynostosis suggest that the hemangiomatous pattern seen in this patient is rare if not unique. The unusual pathological findings provide evidence that the underlying pathophysiology of this disorder may be heterogeneous.


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