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A 14-year-old Nigerian female with idiopathic intracranial hypertension (Pseudotumor cerebri or benign intracranial hypertension)
A 14-year-old secondary school girl presented with acute onset severe generalized headache associated with vomiting and diplopia. These followed an initial fever, which responded to chloroquine. She had been on peflacine for a left knee septic arthritis until onset of her symptoms. The main findings...
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Published in: | African health sciences 2002-12, Vol.2 (3), p.124-126 |
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creator | Onwuchekwa, A C Nwankwo, C N Chapp-Jumbo, E N |
description | A 14-year-old secondary school girl presented with acute onset severe generalized headache associated with vomiting and diplopia. These followed an initial fever, which responded to chloroquine. She had been on peflacine for a left knee septic arthritis until onset of her symptoms. The main findings on physical examination were mild obesity, left abducent nerve palsy, bilateral papilledema and evidence of resolving arthritis of her left knee. The results of her investigations, including a brain CT scan were within normal limits. A diagnosis of IIH was made. She responded satisfactorily to oral acetazolamide with complete resolution of her symptoms and signs within 12 days of hospitalization and 2 weeks of follow-up. |
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These followed an initial fever, which responded to chloroquine. She had been on peflacine for a left knee septic arthritis until onset of her symptoms. The main findings on physical examination were mild obesity, left abducent nerve palsy, bilateral papilledema and evidence of resolving arthritis of her left knee. The results of her investigations, including a brain CT scan were within normal limits. A diagnosis of IIH was made. 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These followed an initial fever, which responded to chloroquine. She had been on peflacine for a left knee septic arthritis until onset of her symptoms. The main findings on physical examination were mild obesity, left abducent nerve palsy, bilateral papilledema and evidence of resolving arthritis of her left knee. The results of her investigations, including a brain CT scan were within normal limits. A diagnosis of IIH was made. She responded satisfactorily to oral acetazolamide with complete resolution of her symptoms and signs within 12 days of hospitalization and 2 weeks of follow-up.</description><subject>Acetazolamide - therapeutic use</subject><subject>Adolescent</subject><subject>Adolescents</subject><subject>Anticonvulsants - therapeutic use</subject><subject>Case Reports</subject><subject>Case studies</subject><subject>Female</subject><subject>Females</subject><subject>Headache Disorders, Secondary - etiology</subject><subject>Health and Medicine</subject><subject>Humans</subject><subject>Medical disorders</subject><subject>Medical treatment</subject><subject>Nigeria</subject><subject>Nigerians</subject><subject>Pseudotumor Cerebri - diagnosis</subject><subject>Pseudotumor Cerebri - drug therapy</subject><issn>1680-6905</issn><issn>1729-0503</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNp1kU9LxDAQxYso7rr6FSQgiB4Kk7RNm4uwLP4DUQ96Lkk63WZpk5q2yh795nZxFRU8zYN58_jNzE4wpSkTISQQ7Y6aZxByAckkOOi6FQDjVND9YEJZmgkQ2TR4nxMah2uUPnR1Qe7NEr2RlpTYyBrJm-krYgrjWtlXRhNjey-1l9bImlTrFn2PtjPOkrPHDofC9UPjPNHoUXlDRqnQmqX9f_D8MNgrZd3h0bbOguery6fFTXj3cH27mN-FLYO0DxOugXJUuoylAgkKlIi0TllURCAiHmHMcdSFAlFoxkTBkkxBTFlcaq1lNAsuPnPbQTVYaNwQ1XnrTSP9OnfS5L871lT50r3mjMY0SbMx4HQb4N3LgF2fN6bTWNfSohu6fDw8QMKS0Xjyx7hyg7fjcvnIxFNBId24jn_yfIN8_Sb6AAmXj3c</recordid><startdate>20021201</startdate><enddate>20021201</enddate><creator>Onwuchekwa, A C</creator><creator>Nwankwo, C N</creator><creator>Chapp-Jumbo, E N</creator><general>Makerere Medical School</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20021201</creationdate><title>A 14-year-old Nigerian female with idiopathic intracranial hypertension (Pseudotumor cerebri or benign intracranial hypertension)</title><author>Onwuchekwa, A C ; Nwankwo, C N ; Chapp-Jumbo, E N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p207t-56c016ebcf4ab0a0b0b93cc723d309363e46e3d3db09dc229d258b04124fccca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Acetazolamide - therapeutic use</topic><topic>Adolescent</topic><topic>Adolescents</topic><topic>Anticonvulsants - therapeutic use</topic><topic>Case Reports</topic><topic>Case studies</topic><topic>Female</topic><topic>Females</topic><topic>Headache Disorders, Secondary - etiology</topic><topic>Health and Medicine</topic><topic>Humans</topic><topic>Medical disorders</topic><topic>Medical treatment</topic><topic>Nigeria</topic><topic>Nigerians</topic><topic>Pseudotumor Cerebri - diagnosis</topic><topic>Pseudotumor Cerebri - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Onwuchekwa, A C</creatorcontrib><creatorcontrib>Nwankwo, C N</creatorcontrib><creatorcontrib>Chapp-Jumbo, E N</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>African health sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Onwuchekwa, A C</au><au>Nwankwo, C N</au><au>Chapp-Jumbo, E N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A 14-year-old Nigerian female with idiopathic intracranial hypertension (Pseudotumor cerebri or benign intracranial hypertension)</atitle><jtitle>African health sciences</jtitle><addtitle>Afr Health Sci</addtitle><date>2002-12-01</date><risdate>2002</risdate><volume>2</volume><issue>3</issue><spage>124</spage><epage>126</epage><pages>124-126</pages><issn>1680-6905</issn><eissn>1729-0503</eissn><abstract>A 14-year-old secondary school girl presented with acute onset severe generalized headache associated with vomiting and diplopia. These followed an initial fever, which responded to chloroquine. She had been on peflacine for a left knee septic arthritis until onset of her symptoms. The main findings on physical examination were mild obesity, left abducent nerve palsy, bilateral papilledema and evidence of resolving arthritis of her left knee. The results of her investigations, including a brain CT scan were within normal limits. A diagnosis of IIH was made. She responded satisfactorily to oral acetazolamide with complete resolution of her symptoms and signs within 12 days of hospitalization and 2 weeks of follow-up.</abstract><cop>Uganda</cop><pub>Makerere Medical School</pub><pmid>12789098</pmid><tpages>3</tpages></addata></record> |
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subjects | Acetazolamide - therapeutic use Adolescent Adolescents Anticonvulsants - therapeutic use Case Reports Case studies Female Females Headache Disorders, Secondary - etiology Health and Medicine Humans Medical disorders Medical treatment Nigeria Nigerians Pseudotumor Cerebri - diagnosis Pseudotumor Cerebri - drug therapy |
title | A 14-year-old Nigerian female with idiopathic intracranial hypertension (Pseudotumor cerebri or benign intracranial hypertension) |
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