Permanent central diabetes insipidus with complete regression of pituitary stalk enlargement after 4 years of follow-up
A 14 year-old patient was admitted because of a history of polyuria and polydipsia. A diagnosis of central diabetes insipidus (CDI) accompanied by growth hormone (GH) and gonadotropin deficiency was made. Hypophyseal magnetic resonance imaging (MRI) of the patient demonstrated isolated pituitary sta...
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| Veröffentlicht in: | Journal of clinical research in pediatric endocrinology 2008, Vol.1 (1), p.38-42 |
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| container_title | Journal of clinical research in pediatric endocrinology |
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| creator | Ocal, Gönül Sıklar, Zeynep Berberoğlu, Merih Bilir, Pelin Engiz, Ozlem Fitoz, Suat Arıcı, Serap |
| description | A 14 year-old patient was admitted because of a history of polyuria and polydipsia. A diagnosis of central diabetes insipidus (CDI) accompanied by growth hormone (GH) and gonadotropin deficiency was made. Hypophyseal magnetic resonance imaging (MRI) of the patient demonstrated isolated pituitary stalk enlargement. Although GH deficiency and gonadotropin deficiency were transient, CDI was persistent despite the regression of the pituitary stalk enlargement over the 4 years of follow-up. |
| doi_str_mv | 10.4008/jcrpe.v1i1.4 |
| format | Article |
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A diagnosis of central diabetes insipidus (CDI) accompanied by growth hormone (GH) and gonadotropin deficiency was made. Hypophyseal magnetic resonance imaging (MRI) of the patient demonstrated isolated pituitary stalk enlargement. Although GH deficiency and gonadotropin deficiency were transient, CDI was persistent despite the regression of the pituitary stalk enlargement over the 4 years of follow-up.</description><identifier>ISSN: 1308-5727</identifier><identifier>EISSN: 1308-5735</identifier><identifier>DOI: 10.4008/jcrpe.v1i1.4</identifier><identifier>PMID: 21318063</identifier><language>eng</language><publisher>Turkey: Galenos Publishing</publisher><subject>Adolescent ; Case Reports ; Diabetes Insipidus, Neurogenic - pathology ; Diabetes Insipidus, Neurogenic - physiopathology ; Humans ; Magnetic Resonance Imaging ; Male ; Pituitary Gland - pathology ; Pituitary Gland - physiopathology</subject><ispartof>Journal of clinical research in pediatric endocrinology, 2008, Vol.1 (1), p.38-42</ispartof><rights>Journal of Clinical Research in Pediatric Endocrinology, Published by Galenos Publishing. 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2984-7b4ed5ce9e2d51ee3fa49d6058cb988aabedd6f46d71bf968019252df8caef763</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005636/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005636/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,4010,27900,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21318063$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ocal, Gönül</creatorcontrib><creatorcontrib>Sıklar, Zeynep</creatorcontrib><creatorcontrib>Berberoğlu, Merih</creatorcontrib><creatorcontrib>Bilir, Pelin</creatorcontrib><creatorcontrib>Engiz, Ozlem</creatorcontrib><creatorcontrib>Fitoz, Suat</creatorcontrib><creatorcontrib>Arıcı, Serap</creatorcontrib><title>Permanent central diabetes insipidus with complete regression of pituitary stalk enlargement after 4 years of follow-up</title><title>Journal of clinical research in pediatric endocrinology</title><addtitle>J Clin Res Pediatr Endocrinol</addtitle><description>A 14 year-old patient was admitted because of a history of polyuria and polydipsia. A diagnosis of central diabetes insipidus (CDI) accompanied by growth hormone (GH) and gonadotropin deficiency was made. Hypophyseal magnetic resonance imaging (MRI) of the patient demonstrated isolated pituitary stalk enlargement. Although GH deficiency and gonadotropin deficiency were transient, CDI was persistent despite the regression of the pituitary stalk enlargement over the 4 years of follow-up.</description><subject>Adolescent</subject><subject>Case Reports</subject><subject>Diabetes Insipidus, Neurogenic - pathology</subject><subject>Diabetes Insipidus, Neurogenic - physiopathology</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Pituitary Gland - pathology</subject><subject>Pituitary Gland - physiopathology</subject><issn>1308-5727</issn><issn>1308-5735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkUFv3CAQhVHUKonSvfUcccul3oIBG18iVVHaVIrUHtozwjBsSLBxwN5V_n3s7GbVchiQ5tObxzyEPlOy5oTIr48mDbDeUk_X_ASdU0ZkIWomPhzfZX2GVjk_kvlwXhMhTtFZSRmVpGLnaPcbUqd76Eds5pJ0wNbrFkbI2PfZD95OGe_8-IBN7IYwN3CCTYKcfexxdHjw4-RHnV5wHnV4wtAHnTbQLZLajZAwxy-gU15gF0OIu2IaPqGPTocMq8N9gf5-v_1zc1fc__rx8-bbfWHKRvKibjlYYaCB0goKwJzmja2IkKZtpNSzU2srxytb09Y1lSS0KUVpnTQaXF2xC3S91x2mtgN7-KMaku9myypqr_7v9P5BbeJWMUJExRaBq4NAis8T5FF1PhsIYV5anLKSgtaCcCZn8sueNCnmnMAdp1CilrTUW1pqSUvxGb_819kRfs-GvQI5gJaj</recordid><startdate>2008</startdate><enddate>2008</enddate><creator>Ocal, Gönül</creator><creator>Sıklar, Zeynep</creator><creator>Berberoğlu, Merih</creator><creator>Bilir, Pelin</creator><creator>Engiz, Ozlem</creator><creator>Fitoz, Suat</creator><creator>Arıcı, Serap</creator><general>Galenos Publishing</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>2008</creationdate><title>Permanent central diabetes insipidus with complete regression of pituitary stalk enlargement after 4 years of follow-up</title><author>Ocal, Gönül ; Sıklar, Zeynep ; Berberoğlu, Merih ; Bilir, Pelin ; Engiz, Ozlem ; Fitoz, Suat ; Arıcı, Serap</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2984-7b4ed5ce9e2d51ee3fa49d6058cb988aabedd6f46d71bf968019252df8caef763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Case Reports</topic><topic>Diabetes Insipidus, Neurogenic - pathology</topic><topic>Diabetes Insipidus, Neurogenic - physiopathology</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Pituitary Gland - pathology</topic><topic>Pituitary Gland - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ocal, Gönül</creatorcontrib><creatorcontrib>Sıklar, Zeynep</creatorcontrib><creatorcontrib>Berberoğlu, Merih</creatorcontrib><creatorcontrib>Bilir, Pelin</creatorcontrib><creatorcontrib>Engiz, Ozlem</creatorcontrib><creatorcontrib>Fitoz, Suat</creatorcontrib><creatorcontrib>Arıcı, Serap</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical research in pediatric endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ocal, Gönül</au><au>Sıklar, Zeynep</au><au>Berberoğlu, Merih</au><au>Bilir, Pelin</au><au>Engiz, Ozlem</au><au>Fitoz, Suat</au><au>Arıcı, Serap</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Permanent central diabetes insipidus with complete regression of pituitary stalk enlargement after 4 years of follow-up</atitle><jtitle>Journal of clinical research in pediatric endocrinology</jtitle><addtitle>J Clin Res Pediatr Endocrinol</addtitle><date>2008</date><risdate>2008</risdate><volume>1</volume><issue>1</issue><spage>38</spage><epage>42</epage><pages>38-42</pages><issn>1308-5727</issn><eissn>1308-5735</eissn><abstract>A 14 year-old patient was admitted because of a history of polyuria and polydipsia. 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| fulltext | fulltext |
| identifier | ISSN: 1308-5727 |
| ispartof | Journal of clinical research in pediatric endocrinology, 2008, Vol.1 (1), p.38-42 |
| issn | 1308-5727 1308-5735 |
| language | eng |
| recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3005636 |
| source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
| subjects | Adolescent Case Reports Diabetes Insipidus, Neurogenic - pathology Diabetes Insipidus, Neurogenic - physiopathology Humans Magnetic Resonance Imaging Male Pituitary Gland - pathology Pituitary Gland - physiopathology |
| title | Permanent central diabetes insipidus with complete regression of pituitary stalk enlargement after 4 years of follow-up |
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