Results 101 to 110 of about 4,903,700 (215)
Histiocytosis X: Langerhans’ Cell Histiocytosis
Hematology/Oncology Clinics of North America, 1987 Histiocytosis X is a complex and poorly understood entity. Nevertheless, it would appear as if certain themes are found recurrently throughout the literature dealing with this disease and a review of them serves as a useful summary. 1. Problems with Nomenclature.
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Perineurioma‐like EMA‐positive calvarial neoplasms: clinicopathological study of eight cases
Histopathology, Volume 89, Issue 3, Page 544-553, September 2026.Perineurioma‐like, EMA‐positive calvarial neoplasms (PLECN) are a rare group of intraosseous spindle cell tumours that demonstrate overlapping morphologic features of perineurioma and fibroblastic meningioma. These lesions tend to behave indolently but show a propensity for progressive growth.
Raheel Rizwan +9 more
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Hematological Oncology, Volume 44, Issue 5, September 2026.
Jerome Razanamahery +10 more
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EXPRESSION OF ADHESION MOLECULES IN LANGERHANS CELL HISTIOCYTOSIS
, 1993 Expression of adhesion molecules was investigated in six biopsy specimens of Langerhans' cell histiocytosis using immunocytochemistry. Cells with Langerhans' cell histiocytosis morphology were stained for ICAM-1, for the beta-1 integrins alpha-4 (VLA-4 ...
C.D. BARONI +8 more
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Systemic findings of Langerhans cell histiocytosis in neonatal period
Revista de la Facultad de Ciencias de la Salud, 2011 We report an unusual case of mediastinal abcessed mass, with involvement of the lung, thymus and probably bone and hematopoietic system, in a newborn that was diagnosed with Langerhans cell histiocytosis.
Rosalba Días-Castro +6 more
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Langerhans Cell Histiocytosis in a Newborn
Journal of the Chinese Medical Association, 2009 A full-term female baby was admitted to our hospital at the postnatal age of 37 days with generalized vesiculopapular, crateriform skin lesions. Physical examination revealed a well-nourished baby without fever, hepatosplenomegaly or lymphadenopathy. Laboratory examination was normal except for thrombocytosis (platelet count, 970 x 10(3)/microL).
Yang, Tzu-Ying +3 more
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JEADV Clinical Practice, Volume 5, Issue 3, Page 1010-1012, September 2026.
Farhanaz Panjshiri +2 more
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Langerhans cell histiocytosis: a diagnostic dilemma
, 2012 Langerhans cell histiocytosis (LCH) is a rare clonal neoplastic disorder of unknown aetiology which can present with a diverse range of clinical presentations.
Paul L Ryan +5 more
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Langerhans Cell Histiocytosis (Letterer-Siwe disease ) - Report of a case
, 2011 Langerhans cell histiocytosis is a rare disorder that occurs when there aretoo many of type of white blood cell called a Langerhans cell. We describe a3-months infant girl who developed wide spread skin lesions since she was 4days of age. . The diagnosis
BS Elagraa +7 more
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Langerhans Cell Histiocytosis of the Clavicle in a 13-Year-Old Boy
Case Reports in Orthopedics, 2014 Langerhans Cell Histiocytosis (LCH) is a rare neoplasm characterized by abnormal proliferation of histiocytic cells. In this case report, we describe a unique case of a 13-year-old boy who presented to the clinic with an insidious onset of mid-clavicular
Shital N. Parikh +3 more
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