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34 results on '"Unger F"'

33. The comorbidity of anger symptoms with personality disorders in psychiatric outpatients.

Author

Digiuseppe R, McDermut W, Unger F, Fuller JR, Zimmerman M, and Chelminski I

Subjects
Adolescent, Adult, Aged, Aged, 80 and over, Comorbidity, Diagnostic and Statistical Manual of Mental Disorders, Female, Humans, Male, Mental Disorders epidemiology, Middle Aged, Outpatients classification, Outpatients psychology, Personality Disorders epidemiology, Psychiatric Status Rating Scales, Young Adult, Anger physiology, Mental Disorders classification, Mental Disorders diagnosis, Personality Disorders diagnosis
Abstract

Objectives: Although many psychiatric disorders are "emotional" disorders, no disorders exist for which dysfunctional anger is a necessary feature. This study examined whether dysfunctional anger could be considered a diagnosis independent from Personality Disorders., Design: We analyzed data on 1,158 psychiatric outpatients who underwent a semi-structured interview for Axis II disorders and ascertained the co-occurrence of dysfunctional anger and Personality Disorders., Results: The overlap between dysfunctional anger and all Personality Disorders was low. Data analyses showed dysfunctional anger was not well accounted for by Axis II diagnoses., Conclusions: Dysfunctional anger can be viewed by researchers and clinicians as an independent diagnostic entity. The implications of these results for the diagnosis and treatment of patients with anger symptoms is discussed., (© 2011 Wiley Periodicals, Inc.)

Published
2012
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34. Rhabdomyosarcoma of lung arising in congenital cystic adenomatoid malformation.

Author

Ueda K, Gruppo R, Unger F, Martin L, and Bove K

Subjects
Female, Humans, Infant, Lung Neoplasms pathology, Lung Neoplasms therapy, Rhabdomyosarcoma pathology, Rhabdomyosarcoma therapy, Lung abnormalities, Lung Neoplasms complications, Rhabdomyosarcoma complications
Abstract

An asymptomatic congenital cystic adenomatoid malformation of lung discovered at age 18 months, and unchanging for 14 months prior to its removal, was found to harbor a small embryonal rhabdomyosarcoma following excision. With lobectomy and chemotherapy, the tumor-free interval has now exceeded three years. The case represents a well-documented occurrence of malignant tumor arising within a congenital malformation, an association that is unlikely to be the result of chance.

Published
1977
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