Roentgen therapy in Hand-Schuller-Christian and related diseases
نویسندگان
چکیده
منابع مشابه
Hand--schuller--christian Disease.
ENDOCRINOLOGICAL, METABOLIC DISORDERS hypophysis dysfunction diabetes insipidus GENITAL DISORDERS genital dysfunctions puberty, delayed HEMOPOIETIC-LYMPHORETICULAR SYSTEM DISORDERS lymphonodus disorders lymphonodus enlarged, lymphadenopathy spleen, anomalies splenomegaly, hepatosplenomegaly LABORATORY DATA lymphoreticular system, changes histiocytosis, including histiocytoma myelo-erythropoieti...
متن کاملOne Case-report of Hand-Schuller-christian Syndrome in Children
SUMMARY Histiocytosis X is associated with idiopathic Proliferation of histiocytes and infiltration of eosinophils in bone marrow Spleen, Liver and other Soft tissues. Clinically there are three distinct forms: 1 - Eosinophilic granuloma is the most benign and Localized form of the disease. 2- Letterer- Siwe is the most malignant, generalized and fatal form of the disease. 3- Hand- Schul...
متن کاملLong-term Remission following Methotrexate Therapy in a Case of Hand-schuller-christian Disease.
The fatal outcome in the case described was unfortunate but was undoubtedly largely attributable to the patient's respiratory condition. The great difficulty which may be encountered in closing the duodenal stump in the presence of massive infiltration must, however, be stressed. We are indebted to Dr. A. A. Miller for valuable assistance with the pathological studies and for helpful advice. RE...
متن کاملمعرفی یک بیمار مبتلا به هیستیوسیتوزیس ایکس از نوع Hand Schuller Christian disease
The term histiocytosis refers to a group of idiopathic clinics entities characterized by diffuse proliferation of mature histiocytes associated with tumorlike masses of foamy reticuloendothelial cells containing lipoid droplets with variable number of eosinophiles and connective tissue. This cells causes tumorlike masses in the bones and other vicera in the body thus it may have very different ...
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ژورنال
عنوان ژورنال: Acta Radiologica
سال: 1958
ISSN: 0001-6926
DOI: 10.3109/00016925809171627