Gene/Protein
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Symptom
Drug
Enzyme
Compound
Pivot Concepts:
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Target Concepts:
Gene/Protein
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Query: UMLS:C0019621 (
Langerhans cell histiocytosis
)
3,250
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Langerhans cell histiocytosis
(
LCH
) is a rare disorder characterized by clonal expansion of antigen presenting Langerhans cells. Different clinical features can be seen according to the involved organs and systems. Multisystem disease with organ dysfunction is more common in infants, whereas single system disease is usually observed in older children. The disease can affect any system or organ throughout the body.
Thymus
is a rarely involvement site reported in
LCH
and usually is accompanied by skin, bone or lung disease. Here we report a 12-year-old male with thymic involvement by
LCH
clinically mimicking lymphoma.
...
PMID:Thymic Langerhans cell histiocytosis mimicking lymphoma. 1868 Jan 63
Thymus
gland involvement in
Langerhans cell histiocytosis
(
LCH
) is usually part of multi-system disease and may be more common than previously recognized. However, thymic involvement causing an anterior mediastinal mass is an extremely rare presentation of multisystem
LCH
. Here we report a 2-month-old-boy admitted to hospital with a giant anterior mediastinal mass with multisystem
LCH
involving the thymus, lungs, liver and skin. The differential diagnosis of mediastinal mass in children should also include
LCH
, especially multisystem disease.
LCH
should also be kept in mind in the differential diagnosis of skin lesions in infants, even if spontaneous regression occurs.
...
PMID:Multisystem langerhans cell histiocytosis with thymic involvement diagnosed with anterior mediastinal mass in a 2-month-old boy. 2827 18