Results 161 to 170 of about 9,012 (189)
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Congenital self-healing non-Langerhans cell histiocytosis
European Journal of Pediatrics, 1988Clinical, morphological, ultrastructural and immunological studies were performed in a case of congenital self-healing non-Langerhans cell histiocytosis. The patient showed several aspects that have not been published before: a large nodule in the vulvar region, vesiculobullous elements and pneumonia (asymptomatic). The relationship of the vesicles and
R. de Groot +3 more
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A Child with Both Langerhans and Non‐Langerhans Cell Histiocytosis
Pediatric Dermatology, 2002Abstract: The histiocytic syndromes consist of a group of disorders that share in common the proliferation of cells of the monocytic/macrophage lineage. It has been conventional to divide the histiocytoses into two separate groups: Langerhans cell histiocytosis (LCH) and non‐LCH.
Ayelet Shani-Adir +3 more
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Progressive Histiocytosis: Description of a Case of Slow-Course Non-Langerhans Cell Histiocytosis
Dermatology, 2002We describe the case of a 37-year-old male patient who in 1992 started developing a skin eruption characterized by dark red to red-yellow papulonodular lesions that showed no tendency to spontaneous resolution. Visceral organs were not involved and the lipid pattern was basically normal.
R. Caputo +4 more
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Progressive nodular histiocytosis – rare variant of cutaneous non‐Langerhans cell histiocytosis
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2006SummaryProgressive nodular histiocytosis is an extremely rare skin disease is clinically characterized by the coincidence of two distinct lesions, namely, superficial xanthomatous papules up to 5 mm and deep nodules and tumors 1–3 cm. Histologically the nodules represent spindle cell xanthogranulomas.
Heidi Seybold +3 more
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Intracranial non-Langerhans cell histiocytosis presenting as an isolated intraparenchymal lesion
Pediatric Radiology, 2010Non-Langerhans cell histiocytosis in the absence of cutaneous or other organ involvement is very rare. A Caucasian boy age 3 years 11 months presented with episodes of recurrent right-side seizures over 2 weeks. Brain CT and MR imaging showed a single enhancing left frontal lobe lesion.
Stephen B. Wharton +4 more
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Fibroblastic rheumatism: fibromatosis rather than non‐Langerhans cell histiocytosis
Journal of Cutaneous Pathology, 2010Background: Fibroblastic rheumatism is a unique fibro‐proliferative disease affecting the skin and joints. It is characterized by distinctive clinical and histological features related to benign spindle‐shaped cells proliferation. Pediatric reports are scarce in the literature.
Nicole Brousse +4 more
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Primary cerebral non-Langerhans cell histiocytosis: MRI and differential diagnosis
Neuroradiology, 2002We report a young woman with primary cerebral non-Langerhans cell histiocytosis of the juvenile xanthogranuloma family. The clinical course was complicated by extensive infiltration of cranial nerves and meninges and epi- and intramedullary spinal dissemination.
Karsten Voigt +5 more
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Non-Langerhans cell histiocytosis associated with lymphocyte-predominant Hodgkin's disease
Clinical and Experimental Dermatology, 1999We report a 74-year-old man who presented with a rash on the trunk showing clinical and histological features of non-Langerhans cell histiocytosis. Two years after presentation he developed weight loss, lymphadenopathy and hepatosplenomegaly; a diagnosis of lymphocyte-predominant Hodgkin's disease was made on lymph node biopsy.
Ibbotson, S. H. +3 more
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Endolymphatic Non-Langerhans Cell Histiocytosis of the Larynx
Journal of Pediatric Hematology/Oncology, 2010We report on an uncommon laryngeal non-Langerhans cell histiocytosis. An 11-year-old boy presented with a 6 months history of progressive breath inhibition. Magnetic resonance imaging showed diffuse laryngeal and local lymph node swelling. Histology first resembled sarcoidosis, however, corticosteroids were ineffective.
Dieter Haffner +4 more
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