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77 Possible Causes for Lymph Node Hyperplasia, Triple A Syndrome

  • 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 ] 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]

  • Diffuse Large B-Cell Lymphoma

    PCDH10 hypermethylation were found in 54.2% (58/107) of DLBCL cases, but only 12.5% (1/8) in reactive lymph node/follicular hyperplasia.[ncbi.nlm.nih.gov] (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] Lymph node biopsy showed reactive lymphoid hyperplasia (RH) with monoclonal proliferation of Epstein-Barr virus (EBV). Her lymphadenopathy regressed without treatment.[ncbi.nlm.nih.gov]

  • 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]

  • 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]

  • 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 (SPART Single Gene Test) (1 gene) Tuberous Sclerosis NGS Panel (2 genes) Tumor Necrosis Factor Receptor-associated[fulgentgenetics.com]

  • POEMS Syndrome

    node hyperplasia), increased levels of serum vascular endothelial growth factor (VEGF), organomegaly, endocrinopathy, edema, typical skin changes, and papilledema. [1] Solitary[ncbi.nlm.nih.gov] We present a patient with POEMS syndrome who achieved rapid complete response to triple therapy consisting of lenalidomide, cyclophosphamide and prednisone, followed by high-dose[ncbi.nlm.nih.gov] When a biopsy is done, these swollen lymph nodes may show Castleman’s Disease (angiofollicular lymph node hyperplasia) or Castleman-like features.[rarediseases.org]

  • Acroosteolysis Dominant Type

    Node Hyperplasia Angiogram for Coronary Artery Disease, Deciding About angioimmunoblastic lymphadenopathy with dysproteinemia Angioimmunoblastic T-Cell Lymphoma Angiokeratoma[healthmedicinet.com] , see triple A syndrome Achalasia-Addisonianism-Alacrima syndrome , see triple A syndrome Achalasia-alacrima syndrome , see triple A syndrome achondrogenesis achondrogenesis[mygenomics.com] Taking Charge of Your Angina, Unstable Angina: Living with a pacemaker or ICD Angio-Osteohypertrophy Syndrome Angioedema and Urticaria Angioedema, Hereditary Angiofollicular Lymph[healthmedicinet.com]

  • Autoimmune Lymphoproliferative Syndrome Type 3

    Lymph nodes showed marked paracortical hyperplasia.[unboundmedicine.com] Trimethadion-Syndrom Trimus-Pseudokamptodaktylie-Syndrom / Hecht-Syndrom Triple-A-Syndrom (Achalasie) Triplo-X-Syndrom Troisier-Hanot-Chauffard-Syndrom Troyer-Syndrom Trypsinogenmangel-Syndrom[schwingfeld.de] Histopathologic examination of left axillary lymph nodes showed reactive follicular hyperplasia with regular distribution of T- and B-dependent areas.[bmcimmunol.biomedcentral.com]

  • Roifman Syndrome

    Hermansky-Pudlak-Syndrom Herrmann-Aguilar-Sacks-Syndrom Herz-Hand-Syndrom HHH-Syndrom (Triple-H-Syndrom) Hirnlokales Syndrom s.[de.wikipedia.org] Trimethadion-Syndrom Trimus-Pseudokamptodaktylie-Syndrom / Hecht-Syndrom Triple-A-Syndrom ( Achalasie ) Triplo-X-Syndrom Troisier-Hanot-Chauffard-Syndrom Troyer-Syndrom Trypsinogenmangel-Syndrom[krankheiten.de] Townes-Brocks-Syndrom Toxisch-embolisches Syndrom Toxisches Schock-Syndrom Treacher-Collins-Syndrom (Franceschetti-Syndrom) Tricho-Dento-Ossäres-Syndrom / TDO-Syndrom (Robinson-Miller-Worth-Syndrom[bionity.com]

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