Results 171 to 180 of about 9,762 (221)

An unusual case of non-Langerhans cell histiocytosis

Journal of the American Academy of Dermatology, 1994
A 28-month-old boy had firm, red nodules for 4 months that were mostly localized to the face. The eruption was preceded by conjunctivitis, eyelid edema, and swelling of the root of the nose. He also had dyspnea, anisocoria with areflexia, swelling of the parotid glands, and hepatosplenomegaly. A bone marrow aspirate showed 25% eosinophils.
R, Caputo, R, Grimalt, E, Ermacora, S, Cavicchini, D, Portaleone   +4 more
openaire   +2 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.
Matthias, Lüftl, Heidi, Seybold, Miklós, Simon, Walter, Burgdorf   +3 more
openaire   +2 more sources

Fibroblastic rheumatism: fibromatosis rather than non‐Langerhans cell histiocytosis

Journal of Cutaneous Pathology, 2010
Background: 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.
Nicolas, Kluger, Alexandra, Dumas-Tesici, Dominique, Hamel, Nicole, Brousse, Sylvie, Fraitag   +4 more
openaire   +2 more sources

Progressive Histiocytosis: Description of a Case of Slow-Course Non-Langerhans Cell Histiocytosis

Dermatology, 2002
We 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, A. Brezzi, G. Vaccari, S. Cavicchini, R. Gianotti   +4 more
openaire   +2 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.
U, Ernemann, M, Skalej, M, Hermisson, M, Platten, R, Jaffe, K, Voigt   +5 more
openaire   +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, Pauline, Chou, Elaine, Morgan, Anthony J, Mancini   +3 more
openaire   +2 more sources

Suprasellar non-Langerhans cell histiocytosis (Erdheim–Chester disease)—a case report

Clinical Imaging, 2013
Erdheim-Chester disease (ECD) is an uncommon non-Langerhans cell histiocytosis that affects multiple body systems and can present clinically in a myriad of ways. An adult onset is most common with bony involvement and constitutional symptoms. We report the case of a 52-year-old female presenting with diabetes insipidus and a suprasellar mass on imaging,
Manas, Sharma, Beth, Vettiyil, Eric, Bartlett, Eugene, Yu   +3 more
openaire   +2 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.
Smitha, Rajaram, Stephen B, Wharton, Fiona, Shackley, Ashok, Raghavan, Daniel J A, Connolly   +4 more
openaire   +2 more sources

Non-Langerhans cell histiocytosis associated with lymphocyte-predominant Hodgkin's disease

Clinical and Experimental Dermatology, 1999
We 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.
null Ibbotson, null Sviland, null Slater, null Reynolds   +3 more
openaire   +4 more sources

Endolymphatic Non-Langerhans Cell Histiocytosis of the Larynx

Journal of Pediatric Hematology/Oncology, 2010
We 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.
Carl Friedrich, Classen, Dieter, Haffner, Horst, Nizze, Peter, Möller, Friedrich, Prall   +4 more
openaire   +2 more sources