1.A clinical study on histiocytosis X.
Sang Oh NA ; Joong Gon KIM ; Hyo Seop AHN
Journal of the Korean Pediatric Society 1989;32(11):1510-1519
No abstract available.
Histiocytosis*
;
Histiocytosis, Langerhans-Cell*
2.Infantile Scabies Masquerading as Langerhans Cell Histiocytosis.
Yoon Seok YANG ; Yun Sun BYUN ; Jin Hye KIM ; Hye One KIM ; Chun Wook PARK
Annals of Dermatology 2015;27(3):349-351
No abstract available.
Histiocytosis, Langerhans-Cell*
;
Scabies*
3.A Case of Letterer-Siwe Disease.
Suh Hong HA ; Jeong Sil HAN ; Sung Won KIM ; Kyung Tae KIM ; Kil Hyun KIM ; Chung Hee CHI
Journal of the Korean Pediatric Society 1987;30(3):335-341
No abstract available.
Histiocytosis, Langerhans-Cell*
4.Histiocytosis-X with Chronic Weeping Ulcers in the Anogenital Areas.
Young Ho SANG ; In Chul CHOI ; Jae Bok JUN ; Do Won KIM ; Sang Lip CHUNG
Annals of Dermatology 1990;2(2):128-131
No abstract available.
Histiocytosis, Langerhans-Cell*
;
Ulcer*
5.Bronchial Washing Cytology of Pulmonary Langerhans Cell Histiocytosis: A Case Report.
Taeyeong KIM ; Hyeong Ju KWON ; Minseob EOM ; Sang Wook KIM ; Min Hi SIN ; Soon Hee JUNG
Journal of Pathology and Translational Medicine 2017;51(4):444-447
No abstract available.
Histiocytosis, Langerhans-Cell*
6.Gastric Langerhans Cell Histiocytosis: Case Report and Review of the Literature.
So Jung LEE ; Chung Su HWANG ; Gi Young HUH ; Chang Hun LEE ; Do Youn PARK
Journal of Pathology and Translational Medicine 2015;49(5):421-423
No abstract available.
Histiocytosis, Langerhans-Cell*
7.A Case of Report of Letterer-Siwe Disease.
Nam Heon KIM ; Jung Ho LEE ; In Ho KIM ; Churl Young CHUNG ; Jong Eun JOO ; Ill Hyang KO
Journal of the Korean Pediatric Society 1981;24(12):1213-1217
No abstract available.
Histiocytosis, Langerhans-Cell*
8.Recent Updates in Langerhans Cell Histiocytosis
Kyung Nam KOH ; Ho Joon IM ; Jong Jin SEO
Clinical Pediatric Hematology-Oncology 2015;22(1):15-21
Langerhans cell histiocytosis (LCH) encompasses a wide range of clinical presentation and its clinical course varies widely from spontaneous regression to severe disseminated disease with the risk of permanent consequences. Although pathogenesis of LCH has been a conundrum, recent advances have led to a better understanding of the molecular pathogenesis of the disease. Especially, advanced genomic analyses have suggested that LCH is a disorder of MAPK pathway mutations. Optimal treatment for LCH has not been established yet. Histiocyte Society has launched a new international multi-center clinical trial, LCH-IV to solve remaining major issues in the treatment of LCH. The aim of this review is to provide an overview of recent understandings on the pathogenesis and treatment of LCH.
Histiocytes
;
Histiocytosis, Langerhans-Cell
10.Idiopathic thrombocytopenic purpura in childhood, Langerhans cell histiocytosis in adulthood: More than a chance association?
Kuan Yueh Chien ; Nurain Mohd Noor
The Medical Journal of Malaysia 2017;72(1):50-52
Described herein, a case of Langerhans cell histiocytosis
(LCH) in an adult with Idiopathic Thrombocytopenic Purpura
(ITP) diagnosed at age ten. She presented with cranial
diabetes insipidus, later developed hypogonadotrophic
hypogonadism and multiple cervical lympadenopathy from
which histopathology of excisional biopsy confirmed LCH.
Magnetic resonance imaging showed thickened pituitary
stalk. Association of ITP and LCH is unknown but the
question of LCH presenting as isolated thrombocytopenia in
childhood only to be discovered in adulthood when there
was pituitary and bone involvement remains. It
reemphasizes the need for high index of suspicion and the
challenges in diagnosing LCH at the outset.
Histiocytosis, Langerhans-Cell
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