Results 191 to 200 of about 14,015 (245)
Some of the next articles are maybe not open access.
Dermatology, 1980
Histiocytosis X is characterized by a proliferation of cytologically benign histiocytes and occurs in a severe form (type 1) with a short course and poor prognosis and a milder form (type 2) with a protracted course and favorable prognosis. Otolaryngologists will encounter the type 2 form of the disease and must include it in the differential diagnosis
Harold F. Schuknecht, Spyros Papaspyrou
+7 more sources
Histiocytosis X is characterized by a proliferation of cytologically benign histiocytes and occurs in a severe form (type 1) with a short course and poor prognosis and a milder form (type 2) with a protracted course and favorable prognosis. Otolaryngologists will encounter the type 2 form of the disease and must include it in the differential diagnosis
Harold F. Schuknecht, Spyros Papaspyrou
+7 more sources
Annals of African Medicine, 2009
Histiocytosis X (Langerhan’s cell granulomatosis) is a disease of unknown aetiology, but viral origin has been implicated.1 It is a clinicopathologic entitycharacterized by proliferation of Langerhan’s cell (which are not primarily phagocytic) in an appropriate milieu ...
Mohammed, A. +4 more
openaire +3 more sources
Histiocytosis X (Langerhan’s cell granulomatosis) is a disease of unknown aetiology, but viral origin has been implicated.1 It is a clinicopathologic entitycharacterized by proliferation of Langerhan’s cell (which are not primarily phagocytic) in an appropriate milieu ...
Mohammed, A. +4 more
openaire +3 more sources
Human Pathology, 1983
To clarify salient issues pertaining to histiocytosis X--a syndrome that includes Letterer-Siwe disease, Hand-Schuller-Christian disease, and eosinophilic granuloma--the authors review the epidemiologic data and the histologic, morphologic, and clinical bases for diagnosis and prognosis. Histiocytes are defined and their possible histogenesis outlined,
B E, Favara, R C, McCarthy, G W, Mierau
openaire +2 more sources
To clarify salient issues pertaining to histiocytosis X--a syndrome that includes Letterer-Siwe disease, Hand-Schuller-Christian disease, and eosinophilic granuloma--the authors review the epidemiologic data and the histologic, morphologic, and clinical bases for diagnosis and prognosis. Histiocytes are defined and their possible histogenesis outlined,
B E, Favara, R C, McCarthy, G W, Mierau
openaire +2 more sources
Otolaryngologic Clinics of North America, 1982
Histiocytosis X may be isolated or generalized in its clinical involvement. Spontaneous resolution may occur, although progression to diffuse systemic disease has also been found. The disease is believed to originate from the mononuclear phagocytic series of cells, although the reason for this activation remains unknown. A possible local reaction to an
M B, Nolph, G A, Luikin
openaire +2 more sources
Histiocytosis X may be isolated or generalized in its clinical involvement. Spontaneous resolution may occur, although progression to diffuse systemic disease has also been found. The disease is believed to originate from the mononuclear phagocytic series of cells, although the reason for this activation remains unknown. A possible local reaction to an
M B, Nolph, G A, Luikin
openaire +2 more sources
Histiocytosis x of the hypothalamus [PDF]
Journal of Endocrinological Investigation, 1991 An unusual case of cutaneous and hypothalamic histiocytosis X (HX) is reported. The hypothalamic involvement occurred as a tumor that mimicked a chiasm glioma on computed tomography angioscanning. Magnetic resonance imaging after gadolinium injection localized the tumor within the third ventricle floor.
M. Dautheribes +7 more
openaire +2 more sources
Archives of Pediatrics & Adolescent Medicine, 1971
1. The clinical, histological and radiological findings in 129 cases of histiocytosis X have been reviewed and the natural history of the disease is discussed. 2. Certain clinical and histological factors emerge as having prognostic significance. 3. The treatment in thirty-four personally reviewed cases is discussed and some suggestions are made as ...
openaire +4 more sources
1. The clinical, histological and radiological findings in 129 cases of histiocytosis X have been reviewed and the natural history of the disease is discussed. 2. Certain clinical and histological factors emerge as having prognostic significance. 3. The treatment in thirty-four personally reviewed cases is discussed and some suggestions are made as ...
openaire +4 more sources
Histiocytosis X: VIII. Histiocytosis X Simulating Tuberculosis
Acta Radiologica: Oncology, 1983The findings in 9 patients with histiocytosis X localized to the spine and 7 patients with tuberculous spondylitis were compared. It was not always possible to differentiate between these two conditions without a supplementary fine needle aspiration biopsy.
N. Bartholdy, E. Bunger, P. Thommesen
openaire +2 more sources
Obstetrics & Gynecology, 1995
Histiocytosis X, a clinically heterogeneous infiltrating disorder, is rarely associated with pregnancy. Diabetes insipidus is a common manifestation of histiocytosis X.A 27-year-old pregnant woman was diagnosed with histiocytosis X by biopsy. At 31 weeks' gestation, she developed diabetes insipidus and required treatment with intranasal 8-D-arginine ...
Howard A. Lippes +4 more
openaire +3 more sources
Histiocytosis X, a clinically heterogeneous infiltrating disorder, is rarely associated with pregnancy. Diabetes insipidus is a common manifestation of histiocytosis X.A 27-year-old pregnant woman was diagnosed with histiocytosis X by biopsy. At 31 weeks' gestation, she developed diabetes insipidus and required treatment with intranasal 8-D-arginine ...
Howard A. Lippes +4 more
openaire +3 more sources
Human Pathology, 1983
The histologic and clinical features of pulmonary histiocytosis X are discussed. The majority of patients are in the third and fourth decades of life. They present with nonspecific respiratory complaints and bilateral reticulonodular infiltrates that can be seen on chest radiographs.
Thomas V. Colby, Charles M. Lombard
openaire +3 more sources
The histologic and clinical features of pulmonary histiocytosis X are discussed. The majority of patients are in the third and fourth decades of life. They present with nonspecific respiratory complaints and bilateral reticulonodular infiltrates that can be seen on chest radiographs.
Thomas V. Colby, Charles M. Lombard
openaire +3 more sources