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65 Possible Causes for Lymph Node Hyperplasia, Triple A Syndrome

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  • Esophageal Metastasis

    Hyaline-vascular and plasma-cell types of giant lymph node hyperplasia of the mediastinum and other locations. Cancer . 1972; 29 :670-683. [ PubMed ] [ DOI ] 6.[wjgnet.com] World J Gastrointest Oncol 2017; 9(9): 397-401 INTRODUCTION Castleman’s disease (CD), which is otherwise known as angiofollicular hyperplasia of the lymph node, is a rare[wjgnet.com] Cervical Castleman’s disease mimicking lymph node metastasis of esophageal carcinoma.[wjgnet.com]

  • Dermatofibrosarcoma Protuberans

    However histopathological examination of these lymph nodes revealed only reactive hyperplasia.[ijdvl.com] (45,X) Trisomy / tetrasomy , other karyotypes / mosaics Klinefelter syndrome (47,XXY) XXYY syndrome (48,XXYY) XXXY syndrome (48,XXXY) 49,XXXYY 49,XXXXY Triple X syndrome[en.wikipedia.org] […] deletion syndrome 22 22q13 deletion syndrome 22 genomic imprinting Angelman syndrome / Prader–Willi syndrome ( 15 ) Distal 18q- / Proximal 18q- X / Y linked Monosomy Turner syndrome[en.wikipedia.org]

  • Multiple Myeloma

    DISCUSSION OF CASE 2 Giant lymph node hyperplasia or Castleman¿s disease (CD) is a heterogeneous clinicopathological entity included in the group of atypical lymphoproliferative[revistanefrologia.com] (45,X) Trisomy / tetrasomy , other karyotypes / mosaics Klinefelter syndrome (47,XXY) XXYY syndrome (48,XXYY) XXXY syndrome (48,XXXY) 49,XXXYY 49,XXXXY Triple X syndrome[en.wikipedia.org] […] deletion syndrome 22 22q13 deletion syndrome 22 genomic imprinting Angelman syndrome / Prader–Willi syndrome ( 15 ) Distal 18q- / Proximal 18q- X / Y linked Monosomy Turner syndrome[en.wikipedia.org]

  • Spondylometaphyseal Dysplasia with Combined Immunodeficiency

    47,XXX see triple X syndrome XXX syndrome see triple X syndrome 47,XXY see Klinefelter syndrome XXY syndrome see Klinefelter syndrome XXY trisomy see Klinefelter syndrome[urinator.com] […] imperfecta#Type I triple X syndrome X Triplo X syndrome see triple X syndrome X Trisomy 21 see Down syndrome Trisomy X see triple X syndrome X Troisier-Hanot-Chauffard syndrome[debatingchristianity.com] SUDS : See Brugada syndrome. Super Female : See Triple X Syndrome. Superficial Siderosis : Superficial Siderosis is categorized as a rare disease. Sup...[psychforums.com]

  • Nakajo Syndrome

    node hyperplasia (Castleman disease), CNS abnormalities (eg, hypothalamic dysfunction), drug fever, factitious fever, IgG4-related disease, immunodeficiency syndromes with[cfp.ca] , see triple A syndrome Achalasia-Addisonianism-Alacrima syndrome , see triple A syndrome Achalasia-alacrima syndrome , see triple A syndrome achondrogenesis achondrogenesis[mygenomics.com] A Syndrome (AAAS Single Gene Test) (1 gene) Troyer Syndrome (SPG20 Single Gene Test) (1 gene) Tuberous Sclerosis NGS Panel (2 genes) Tumor Necrosis Factor Receptor-associated[fulgentgenetics.com]

  • Peripheral Motor Neuropathy - Dysautonomia Syndrome

    Page 68 Castleman’s Disease Chronic Relapsing Neuropathy Associated with Castleman’s Disease (Angiofollicular Lymph Node Hyperplasia) Eur Neurol 1995;35:336-340 Vingerhoets[de.slideshare.net] Mutant WD-repeat protein in triple-A syndrome. Nat Genet 2000 ; 26 : 332 –5. Chu M , Berlin D, Axelrod F.[jnnp.bmj.com] node hyperplasia … Chronic progressive form of neuropathy associated with Castleman’s disease and the Crow-Fukase syndrome. - Unicentrische of multicentrische lymfadenopathie[de.slideshare.net]

  • Retractile Mesenteritis

    […] follicular hyperplasia in lymph nodes.[saudijgastro.com] 47 RothmundThomson Syndrome 37 Trisomy 18 Syndrome 48 Scleromyxedema 38 Syndrome Triple X Syndrome 49 Setleis Syndrome 39 XXY Syndrome Klinefelter Syndrome 50 Sutton Disease[books.google.com] Two lymph nodes showed a reactive hyperplasia. Final diagnosis was intestinal obstruction by mesenteric fat necrosis with fibrous adhesion.[ejs.eg.net]

  • Acquired Adrenogenital Syndrome

    Back to top The Lymphoid System Lymph Nodes The functional anatomy of lymph nodes. Non-specific reactive hyperplasia.[tcd.ie] 47 RothmundThomson Syndrome 37 Trisomy 18 Syndrome 48 Scleromyxedema 38 Syndrome Triple X Syndrome 49 Setleis Syndrome 39 XXY Syndrome Klinefelter Syndrome 50 Sutton Disease[books.google.de] Trisomy 9p Multiple Variants 44 Pityriasis Rubra Pilaris 34 Chromosome 9 Trisomy Mosaic 45 Pseudoxanthoma Elasticum 35 Pentasomy X 46 Pyoderma Gangrenosum 36 Trisomy 13 Syndrome[books.google.de]

  • Gianotti-Crosti Syndrome

    […] of the lymph nodes, acute hepatitis, usually anicteric, lasting for a minimum period of 2 months and hepatitis B surface antigenemia. [1] Following the initial report, subsequent[ijdvl.com] 47 RothmundThomson Syndrome 37 Trisomy 18 Syndrome 48 Scleromyxedema 38 Syndrome Triple X Syndrome 49 Setleis Syndrome 39 XXY Syndrome Klinefelter Syndrome 50 Sutton Disease[books.google.com] […] of lymph nodes Acute hepatitis, usually anicteric, which could last for months and progress to chronic liver disease 2. to three-quarters of cases in some series [12,24-28[slideshare.net]

  • Aprosencephaly and Cerebellar Dysgenesis

    Node Hyperplasia) Castleman’s Tumor: (see Giant Lymph Node Hyperplasia) Cat Diseases: 0.03, 0.24, 0.70, 17.50, 35.17, 97.50, 222.70, 314.33, 560.00, 707.26, Cat Eye Syndrome[drhuldaclarkzappers.wordpress.com] , see triple A syndrome Achalasia-Addisonianism-Alacrima syndrome , see triple A syndrome Achalasia-alacrima syndrome , see triple A syndrome achondrogenesis achondrogenesis[mygenomics.com] Carrion’s Disease: (see Bartonella Infections) Cartilage Diseases: 0.06, 0.52, 27.50, 55.75, 125.19, 250.00, 354.72, 517.50, 683.00, 712.42, Castleman Disease: (see Giant Lymph[drhuldaclarkzappers.wordpress.com]

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