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Article: Nephrotic syndrome associated with angiofollicular lymph node hyperplasia

TitleNephrotic syndrome associated with angiofollicular lymph node hyperplasia
Authors
Issue Date1987
Citation
Pathology, 1987, v. 19 n. 4, p. 429-432 How to Cite?
AbstractA woman presented at the age of 22 with anemia, hepatosplenomegaly, polyclonal hypergammaglobulinemia and a mediastinal shadow. At thoracotomy she had enlarged mediastinal lymph nodes which displayed histological features typical of angiofollicular hyperplasia. Marrow plasmacytosis was present. She developed diabetes mellitus at the age of 29 yrs after she had received oral steroid treatment for one year. The nephrotic syndrome supervened another year later. Her kidneys were enlarged before the onset of diabetes. The glomerular changes included a marked increase of mesangial matrix and segmental hypercellularity. The association of the nephrotic syndrome and angiofollicular lymph node hyperplasia is extremely rare and their interrelation remains enigmatic.
Persistent Identifierhttp://hdl.handle.net/10722/147803
ISSN
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChan, KWen_US
dc.contributor.authorChan, MKen_US
dc.contributor.authorChoy, DTKen_US
dc.date.accessioned2012-05-29T06:09:18Z-
dc.date.available2012-05-29T06:09:18Z-
dc.date.issued1987en_US
dc.identifier.citationPathology, 1987, v. 19 n. 4, p. 429-432en_US
dc.identifier.issn0031-3205en_US
dc.identifier.urihttp://hdl.handle.net/10722/147803-
dc.description.abstractA woman presented at the age of 22 with anemia, hepatosplenomegaly, polyclonal hypergammaglobulinemia and a mediastinal shadow. At thoracotomy she had enlarged mediastinal lymph nodes which displayed histological features typical of angiofollicular hyperplasia. Marrow plasmacytosis was present. She developed diabetes mellitus at the age of 29 yrs after she had received oral steroid treatment for one year. The nephrotic syndrome supervened another year later. Her kidneys were enlarged before the onset of diabetes. The glomerular changes included a marked increase of mesangial matrix and segmental hypercellularity. The association of the nephrotic syndrome and angiofollicular lymph node hyperplasia is extremely rare and their interrelation remains enigmatic.en_US
dc.languageengen_US
dc.relation.ispartofPathologyen_US
dc.subject.meshAdulten_US
dc.subject.meshDiabetes Mellitus, Type 2 - Complications - Pathologyen_US
dc.subject.meshFemaleen_US
dc.subject.meshGiant Lymph Node Hyperplasia - Complications - Pathologyen_US
dc.subject.meshHumansen_US
dc.subject.meshKidney - Pathologyen_US
dc.subject.meshLymph Nodes - Pathologyen_US
dc.subject.meshNephrotic Syndrome - Complications - Pathologyen_US
dc.titleNephrotic syndrome associated with angiofollicular lymph node hyperplasiaen_US
dc.typeArticleen_US
dc.identifier.emailChan, KW:hrmtckw@hku.hken_US
dc.identifier.authorityChan, KW=rp00330en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.pmid3444667-
dc.identifier.scopuseid_2-s2.0-0023511567en_US
dc.identifier.volume19en_US
dc.identifier.issue4en_US
dc.identifier.spage429en_US
dc.identifier.epage432en_US
dc.identifier.isiWOS:A1987K766600020-

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