A Case of Hemophagocytic Syndrome with Cervical Lymphadenopathy.
نویسندگان
چکیده
منابع مشابه
Autoimmune Lymphoproliferative Syndrome Misdiagnosed as Hemophagocytic Lymphohistiocytosis A Case Report
Autoimmune lymphoproliferative Syndrome (ALPS) is a rare inherited disorder of apoptosis. It usually presents with chronic lymphadenopathy, splenomegaly, and symptomatic cytopenia in a child. Herein, we report a 14-year-old boy with symptoms misdiagnosed as hemophagocytic lymphohistiocytosis who was treated before ALPS was diagnosed for the patient. This case should alert pediatricians to consi...
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Palpable lymphadenopathy is common in children, with studies showing a prevalence of 55% in children aged 6– 12 months and 41% in children aged 2–5 years. The majority of palpable lymph nodes are reactive, and serious pathology is rare. The challenge is to find clinical, radiological and serological evidence that is reliable enough to exclude malignancy (most likely lymphoma). This is a very di...
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Dear Editor, A 42-year-old man presented with a 4-week history of erythematous, maculopapular rash over his whole body (Fig.1), shortness of breath and generalised lymphadenopathy for 1 week. Clinical examination showed erythroderma with multiple lymph nodes in the cervical, axillary and groin areas. The lymph nodes were firm, mobile, non tender and were not attached to underlying structures. T...
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Chediak Higashi syndrome, is a rare autosomal recessive disorder characterised by oculocutaneus albinism, recurrent respiratory system infections and other pyogenic infections. Hemophagocytic lymphohistiocytosis can develop in any time of the life in patients with Chediak Higashi syndrome. A 14-month-old girl patient was diagnosed as hemophagocytic lymphohistiocytosis with the laboratory findin...
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ژورنال
عنوان ژورنال: Practica Oto-Rhino-Laryngologica
سال: 2001
ISSN: 1884-4545,0032-6313
DOI: 10.5631/jibirin.94.469