organomegaly

臓器肥大

Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/06/04 16:47:09」(JST)

wiki en

[Wiki en表示]

Organomegaly is the abnormal enlargement of organs. For example, clitoromegaly is the enlargement of the clitoris, hepatomegaly is enlargement of the liver, cardiomegaly is enlargement of the heart, and splenomegaly is enlargement of the spleen.

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

• 1. POEMS症候群 poems syndrome
• 2. ベックウィズ・ヴィーデマン症候群 beckwith wiedemann syndrome
• 3. ゴーシェ病：初期評価、モニタリング、および臨床経過 gaucher disease initial assessment monitoring and clinical course
• 4. 女性における急性骨盤痛の評価 evaluation of acute pelvic pain in women
• 5. 慢性リンパ性白血病の病期分類および予後 staging and prognosis of chronic lymphocytic leukemia

English Journal

• MRI and MRS findings in fucosidosis; a rare lysosomal storage disease.

• Ediz SS1, Aralasmak A2, Yilmaz TF3, Toprak H3, Yesil G4, Alkan A3.
• Brain & development.Brain Dev.2016 Apr;38(4):435-8. doi: 10.1016/j.braindev.2015.09.013. Epub 2015 Oct 26.
• Fucosidosis is a rare lysosomal storage disorder caused by deficient activity of the enzyme l-fucosidase in all tissues. We presented magnetic resonance imaging [MRI] and MR spectroscopy [MRS] findings of a 4-year-old boy with genetically proven fucosidosis. He had a history and clinical findings of
• PMID 26515723

• Autologous cytokine-induced killer (CIK) cell immunotherapy combined with cyclophosphamide in five patients with POEMS syndrome.

• Ma L1, Wang Y2, Bo J3, Han W2, Wang Y1, Zhang L1, Wu X1, Yu S1, Liu R1.
• Clinical and experimental immunology.Clin Exp Immunol.2016 Apr;184(1):83-9. doi: 10.1111/cei.12755. Epub 2016 Jan 19.
• The primary objective of this study was to evaluate the safety and clinical efficacy of autologous cytokine-induced killer (CIK) cells combined with cyclophosphamide in the treatment of polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes (POEMS) syndrome patients. We
• PMID 26660736

• A Patient With Atypical Multiple Sulfatase Deficiency.

• Miskin C1, Melvin JJ1, Legido A1, Wenger DA2, Harasink SM1, Khurana DS3.
• Pediatric neurology.Pediatr Neurol.2016 Apr;57:98-100. doi: 10.1016/j.pediatrneurol.2015.10.023. Epub 2015 Dec 24.
• BACKGROUND: Multiple sulfatase deficiency is an autosomal recessive lysosomal storage disorder characterized by the absence of several sulfatases and resulting from mutations in the gene encoding the human C (alpha)-formylglycine-generating enzyme. There have been a variety of biochemical and clinic
• PMID 26825355

Japanese Journal

• Coexistence of Quasi-moyamoya Disease and POEMS Syndrome in a Patient with Intracranial Hemorrhage: A Case Report and Literature Review

• NMC Case Report Journal 4(1), 5-9, 2017
• NAID 130005239937

• The first case of POEMS syndrome with synchronous breast cancer: What are the associated diagnostic challenges?

• Clinical Case Reports 4(4), 369-375, 2016-04
• NAID 120005971162

• Diffuse Large B-cell Lymphoma during Corticosteroid Therapy for TAFRO Syndrome

• Internal Medicine 55(19), 2861-2867, 2016
• NAID 130005605843

Related Links

• Organomegaly Medical Definition | Merriam-Webster Medical ...

Seen and Heard What made you want to look up organomegaly? Please tell us where you read or heard it (including the quote, if possible).

• Organomegaly | definition of organomegaly by Medical dictionary

visceromegaly [vis″er-o-meg´ah-le] enlargement of the viscera; called also organomegaly and splanchnomegaly. vis·cer·o·meg·a·ly (vis'ĕr-ō-meg'ă-lē), Abnormal enlargement of the viscera, such as may be seen in acromegaly and other ...

Related Pictures