Studies in Schizophrenia, V.

1959 ◽  
Vol 105 (439) ◽  
pp. 313-325 ◽  
Author(s):  
H. H. Fleischhacker ◽  
J. B. Lancaster ◽  
A. P. Wheeler

The problems of diagnosis, pathogenesis, aetiology and successful treatment of the idiopathic schizophrenias is one of the most urgent and formidable ones which psychiatry has still to tackle. It is most urgent because of the large number of sufferers struck by the disease, made unfit for a successful life at an early age, and the distress imposed on them and their relatives. It is most formidable because our essential knowledge of the nature of this disease, or possibly group of diseases, is scanty and disorderly and opinions are conflicting and contradictory. This unsatisfactory state is made worse by the fact that there is quite an amount of disagreement on diagnosis, so that often the findings of different workers do not refer to comparable groups of patients (and conditions in which they are examined) which must add to the confusion, particularly when metabolic examinations are carried out. Too often “marginal psychoses“, and also not rarely, paranoid hallucinatory states with and without changes of the personality are called “schizophrenia”. The last-named states are not infrequently schizophrenoid reactions (or reactions of a schizoid person) to psychogenic causes or to potentially diagnosable physical disorders. On close clinical examination one would also find that the symptomatology of such cases is not that of idiopathic schizophrenia. In the “classical” schizophrenias of Kraepelin, Bleuler and Kleist, despite some discrepancies, the typical para-functions of feeling, willing, thinking and activity, usually accompanied by hallucinations, mainly auditory, and paranoid delusions are present and also a disturbance of the albumin/globulin ratio in C.S.F. and serum. In the absence of this mental and physical symptomatology the diagnosis of idiopathic schizophrenia should not be made (Fleischhacker et al. (7, 8)).

2006 ◽  
Vol 10 (1) ◽  
pp. 45-47 ◽  
Author(s):  
Diya F. Mutasim

Background: Inflammatory linear verrucous epidermal nevus (ILVEN) is a relatively rare disorder that is characterized by an early age at onset; severely pruritic linear papules and plaques; histologic features resembling spongiotic dermatitis, psoriasis, or lichenified dermatitis; and poor response to treatment. Objective: To report the successful treatment of ILVEN with potent topical steroid and tacrolimus ointments. Methods: An 11-year-old girl presented with a 1-year history of markedly pruritic, progressive linear eruption that extended from the right foot to the right buttock. She had failed treatment with pimecrolimus, calcipotriol, mometasone furoate, triamcinolone, tazarotene, and alpha-hydroxy acid. Histologic examination revealed the findings of spongiotic dermatitis. Results: The lesions resolved with fluocinonide ointment and tacrolimus 0.1% ointment. Conclusion: The combination of two therapeutic agents with different mechanisms of action likely resulted in the successful treatment of this usually resistant condition.


Author(s):  
Bruce Mackay

The broadest application of transmission electron microscopy (EM) in diagnostic medicine is the identification of tumors that cannot be classified by routine light microscopy. EM is useful in the evaluation of approximately 10% of human neoplasms, but the extent of its contribution varies considerably. It may provide a specific diagnosis that can not be reached by other means, but in contrast, the information obtained from ultrastructural study of some 10% of tumors does not significantly add to that available from light microscopy. Most cases fall somewhere between these two extremes: EM may correct a light microscopic diagnosis, or serve to narrow a differential diagnosis by excluding some of the possibilities considered by light microscopy. It is particularly important to correlate the EM findings with data from light microscopy, clinical examination, and other diagnostic procedures.


1982 ◽  
Vol 47 (4) ◽  
pp. 373-375 ◽  
Author(s):  
James L. Fitch ◽  
Thomas F. Williams ◽  
Josephine E. Etienne

The critical need to identify children with hearing loss and provide treatment at the earliest possible age has become increasingly apparent in recent years (Northern & Downs, 1978). Reduction of the auditory signal during the critical language-learning period can severely limit the child's potential for developing a complete, effective communication system. Identification and treatment of children having handicapping conditions at an early age has gained impetus through the Handicapped Children's Early Education Program (HCEEP) projects funded by the Bureau of Education for the Handicapped (BEH).


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