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Cervical vertebra plana secondary to Ewing sarcoma: A case report. [PDF]
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Otolaryngology–Head and Neck Surgery, 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
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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
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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
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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
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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
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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
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Histiocytosis X of the hypothalamus
Neurosurgery, 1989Abstract An 18-year-old woman presented with visual disturbance and endocrine dysfunction (diabetes insipidus, delayed puberty, hypothyroidism, hypoadrenalism, and hyperprolactinemia). Computed tomography and enhanced cisternography showed a single hypothalamic mass, which proved at biopsy to be histiocytosis X.
K P, Ober +4 more
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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.
P, Thommesen, N, Bartholdy, E, Bünger
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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 ...
L A, DiMaggio, H A, Lippes, R V, Lee
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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 ...
L A, DiMaggio, H A, Lippes, R V, Lee
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Hematology/Oncology Clinics of North America, 1987
This article acts as an overview of this issue of Hematology/Oncology Clinics of North America. We discuss the several themes that recur in the research and therefore in this issue concerning histiocytosis-X.
M E, Osband, C, Pochedly
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This article acts as an overview of this issue of Hematology/Oncology Clinics of North America. We discuss the several themes that recur in the research and therefore in this issue concerning histiocytosis-X.
M E, Osband, C, Pochedly
openaire +2 more sources