Familial dementia with Pick's cells – a case report of probable familial Pick's disease

1994 ◽  
Vol 11 (1) ◽  
pp. 34-38 ◽  
Author(s):  
Fiona Gaughran ◽  
Catherine Keohane ◽  
Mary Buckley

AbstractThe clinical and pathological features are described in a case of prolonged dementia in a 59 year old man with familial dementia and extrapyramidal disorder. Postmortem examination showed severe fronto-temporal and basal ganglia atrophy, with many “ballooned neurons” in the residual cortex most likely representing Pick's disease. The differential diagnosis is discussed and aspects of this rare condition are reviewed.

1992 ◽  
Vol 50 (2) ◽  
pp. 216-218
Author(s):  
J. Teotônio de Oliveira ◽  
Francisco E. Cota Cardoso

The case of a Brazilian patient with cortico-basal ganglionic degeneration (CBGD) is presented. Since three years ago, a 71-year old male displays asymmetric ideomotor apraxia, gait apraxia, cortical sensory impairment, myoclonus, limp dystonia and rigidity. His mental status is spared. There is neither consanguinity nor similar cases in his family. The differential diagnosis of CBGD is discussed. A brief review of the literature is made stressing the clinical and pathological features of CBGD. This disease is poorly known and probably underdiagnosed. Its diagnosis can be safely made based on clinical grounds.


1943 ◽  
Vol 89 (374) ◽  
pp. 1-20 ◽  
Author(s):  
E. Stengel

Many problems concerning Alzheimer's disease and Pick's disease are still awaiting clarification. In this country Henderson was the first to draw attention to the considerable importance of Alzheimer's disease in clinical psychiatry. Valuable work has been contributed by various writers in recent years (Grunthal, 1936; Critchley, 1929, 1930, 1931, 1938; Schottky, 1932; Thorpe, 1932; Rothschild, 1934; Malamud, Lowenberg and co-workers, 1929; Mayer-Gross, 1938; Kasanin and Crank, 1933; Jervis and Soltz, 1936; McMenemy, a.o., 1939). While Pick's disease has retained its position as a clinical entity based mainly on the characteristic anatomical picture, the position of Alzheimer's disease in the system of psychiatry has become more complicated; for instance atypical cases have been described presenting the anatomical characters of Alzheimer's disease, though not fitting into the original clinical conception of that disease. Lowenberg and his co-workers (1929) are inclined to regard Alzheimer's disease as a syndrome rather than a clinical entity. Many contributors have directed their main interest to the pathological changes. The knowledge of the symptomatology of those conditions is still incomplete. Further intensive study may enable us not only to base the diagnosis and differential diagnosis of Alzheimer's disease and Pick's disease on more solid clinical knowledge than hitherto, but also to recognize the early stages of those diseases before advancing cerebral degeneration effaces their characteristic clinical features. Unfortunately, most of the cases come under the observation of the psychiatrist only in the later stages of their illness, and it seems that the comparatively small proportion of the mental hospital population they represent does not reflect the incidence of those diseases. It is very likely that many patients die from intercurrent illnesses before their mental condition is recognized or sufficiently advanced to make admission to a mental hospital necessary. The differential diagnosis of those conditions offers considerable difficulties which often may prove insuperable. Alzheimer's disease and Pick's disease have to be distinguished not only from each other but from conditions of vascular origin, from senile dementia and various atypical conditions which occur at the same age period during which Alzheimer's disease and Pick's disease usually develop. Only careful collection and analysis of clinical observations and their scrutiny by pathological investigations can increase our still limited knowledge in this important field of psychiatry.


2011 ◽  
Vol 2011 ◽  
pp. 1-3
Author(s):  
Klaus Steinbrück ◽  
Marcelo Enne ◽  
Reinaldo Fernandes ◽  
Jose M. Martinho ◽  
Lúcio F. Pacheco-Moreira

Inflammatory pseudotumor of the liver (IPTL) is a rare condition, but an important differential diagnosis of hepatic space-occupying lesions. It may regress spontaneously and mimic other liver tumors. Complications are usually intrahepatic. Herein, we present a case of IPTL which developed pleural empyema and lung necrosis as an uncommon complication.


1987 ◽  
Vol 73 (2) ◽  
pp. 115-117
Author(s):  
M. N. Jeffrey ◽  
M. J. Jeffrey

AbstractA case of conjunctival amyloid in a 56 year old lady is described in whom no evidence of predisposing localised or systemic disease was found. Histochemistry and immunocytochemistry showed that the amyloid was immunoglobulin-derived. The clinical and pathological features of conjunctival amyloid are discussed.


1988 ◽  
Vol 83 (1) ◽  
pp. 63-74 ◽  
Author(s):  
Ichiro Kanazawa ◽  
Shin Kwak ◽  
Hidenao Sasaki ◽  
Osamu Muramoto ◽  
Toshio Mizutani ◽  
...  

1999 ◽  
Vol 19 (4) ◽  
pp. 370-379 ◽  
Author(s):  
Kuniaki Tsuchiya ◽  
Kunimasa Arima ◽  
Toshiya Fukui ◽  
Toshihiko Kuroiwa ◽  
Chie Haga ◽  
...  

1993 ◽  
Vol 38 (5) ◽  
pp. 368-369
Author(s):  
Emmanuel Stip ◽  
Jocelyne Coumoyer ◽  
Pierre Léouffre ◽  
Gérard Cournoyer

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