Results 91 to 100 of about 12,716 (134)

Generalized indeterminate cell histiocytosis successfully treated with methotrexate

JAAD Case Reports, 2022
Erina Lie, MD, Jaroslaw Jedrych, MD, Ronald Sweren, MD, Michelle L. Kerns, MD   +3 more
doaj  

Erdheim-Chester Disease (ECD) is a Rare Histiocytic Neoplasm of Non-Langerhans Cell Histiocytosis [PDF]

Abdalla Bowirrat, Aia Bowirrat, Bowirrat Ann   +2 more
openalex   +1 more source

Bone Langerhans cell histiocytosis with pulmonary involvement in an adult non-smoker: A case report and brief review of the literature

, 2016
Jie Shen, Shicheng Feng
openalex   +2 more sources

A Child with Both Langerhans and Non‐Langerhans Cell Histiocytosis

Pediatric Dermatology, 2002
Abstract: 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, Elaine Morgan, Pauline Chou, Anthony J. Mancini   +3 more
semanticscholar   +5 more sources

Progressive nodular histiocytosis – rare variant of cutaneous non‐Langerhans cell histiocytosis

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2006
SummaryProgressive 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, Walter H.C. Burgdorf, Miklós Simon, Matthias Lüftl   +3 more
semanticscholar   +5 more sources

Diffuse xanthogranulomatous dermatitis and systemic Langerhans cell histiocytosis: A novel case that demonstrates bridging between non-Langerhans cell histiocytosis and Langerhans cell histiocytosis

Journal of the American Academy of Dermatology, 2009
The advent of electron microscopy and immunohistochemical stains allowed for reclassification of the histiocytoses based on the predominant cell in the infiltrate. Although the current schema simplicity provides a good foundation, some patients display overlapping clinical and immunohistochemical features that defy classification.
Elizabeth K. Satter, Sarah B. Gendernalik, Kenneth J. Galeckas   +2 more
semanticscholar   +5 more sources

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Non-Langerhans cell histiocytosis

Acta Neurologica Belgica, 2016
A 34-year-old man complained of seizures, headache and reduced visual acuity for a month. Physical examination revealed intracranial hypertension. CSF showed high opening pressure, increase of protein (121 mg/dl) and 26 leukocytes per mm, 94 % of which were lymphomononuclear cells, with cytoplasmic and nuclear atypia.
Lívia Nathália Alaite Silveira, Luciano de Souza Queiroz, Fabiano Reis   +2 more
openaire   +3 more sources

Congenital self-healing non-Langerhans cell histiocytosis

European Journal of Pediatrics, 1988
Clinical, 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, M. E. F. Prins, V. D. Vuzevski, Arnold P. Oranje   +3 more
openaire   +4 more sources

Intracranial non-Langerhans cell histiocytosis presenting as an isolated intraparenchymal lesion

Pediatric Radiology, 2010
Non-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, Fiona Shackley, Daniel J. A. Connolly, Ashok Raghavan, Smitha Rajaram   +4 more
openaire   +4 more sources

Primary cerebral non-Langerhans cell histiocytosis: MRI and differential diagnosis

Neuroradiology, 2002
We 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, R. Jaffe, M. Hermisson, Ulrike Ernemann, Martin Skalej, Michael Platten   +5 more
openaire   +4 more sources