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Primary hydatidosis of the central nervous system: A retrospective study of 39 Tunisian cases

Abstract Objective To analyze epidemiological characteristics, clinical symptoms, radiological aspects, treatment and outcome of central nervous system hydatidosis and compare our results with those reported in literature. Patients and methods In our retrospective study, we reviewed 39 cases of prim...

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Published in:Clinical neurology and neurosurgery 2010-01, Vol.112 (1), p.23-28
Main Authors: Limaiem, Faten, Bellil, Selma, Bellil, Khadija, Chelly, Inès, Mekni, Amina, Khaldi, Moncef, Haouet, Slim, Zitouna, Moncef, Kchir, Nidhameddine
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container_issue 1
container_start_page 23
container_title Clinical neurology and neurosurgery
container_volume 112
creator Limaiem, Faten
Bellil, Selma
Bellil, Khadija
Chelly, Inès
Mekni, Amina
Khaldi, Moncef
Haouet, Slim
Zitouna, Moncef
Kchir, Nidhameddine
description Abstract Objective To analyze epidemiological characteristics, clinical symptoms, radiological aspects, treatment and outcome of central nervous system hydatidosis and compare our results with those reported in literature. Patients and methods In our retrospective study, we reviewed 39 cases of primary central nervous system hydatid cysts operated on in our hospital between 1998 and 2007. Results There were 20 male and 19 female patients (sex-ratio M/F = 1.05) between 2 and 68 years of age (mean = 26.5 years). Thirteen of the patients were children (33.3%) with a mean age of 6.8 years and 26 were adults (66.7%) with a mean age of 36.3 years. The location of hydatid cysts was intracranial in 27 cases (69.2%) and spinal in 12 cases (30.8%). Headache and motor deficits were the predominant symptoms in patients with intracranial hydatidosis whereas back pain and spinal cord compression syndrome were the most frequent clinical presentations in patients with spinal hydatidosis. All patients underwent surgical resection of the cyst. Pathologic findings were consistent with hydatid cyst in all cases. During the follow-up period which ranged between 12 months and 5 years, 12 patients had recurrence (30.7%). Only one patient with intracranial hydatid cyst died postoperatively due to anaphylactic shock. Conclusion Despite all the advances in imaging techniques and therapeutic methods, central nervous system hydatidosis remains difficult to cure and patient outcomes are not satisfactory especially in case of spinal involvement due to the high incidence of recurrence.
doi_str_mv 10.1016/j.clineuro.2009.09.001
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Patients and methods In our retrospective study, we reviewed 39 cases of primary central nervous system hydatid cysts operated on in our hospital between 1998 and 2007. Results There were 20 male and 19 female patients (sex-ratio M/F = 1.05) between 2 and 68 years of age (mean = 26.5 years). Thirteen of the patients were children (33.3%) with a mean age of 6.8 years and 26 were adults (66.7%) with a mean age of 36.3 years. The location of hydatid cysts was intracranial in 27 cases (69.2%) and spinal in 12 cases (30.8%). Headache and motor deficits were the predominant symptoms in patients with intracranial hydatidosis whereas back pain and spinal cord compression syndrome were the most frequent clinical presentations in patients with spinal hydatidosis. All patients underwent surgical resection of the cyst. Pathologic findings were consistent with hydatid cyst in all cases. During the follow-up period which ranged between 12 months and 5 years, 12 patients had recurrence (30.7%). Only one patient with intracranial hydatid cyst died postoperatively due to anaphylactic shock. Conclusion Despite all the advances in imaging techniques and therapeutic methods, central nervous system hydatidosis remains difficult to cure and patient outcomes are not satisfactory especially in case of spinal involvement due to the high incidence of recurrence.</description><identifier>ISSN: 0303-8467</identifier><identifier>EISSN: 1872-6968</identifier><identifier>DOI: 10.1016/j.clineuro.2009.09.001</identifier><identifier>PMID: 19781849</identifier><identifier>CODEN: CNNSBV</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adolescent ; Adult ; Aged ; Biological and medical sciences ; Brain - diagnostic imaging ; Brain - pathology ; Central nervous system ; Central Nervous System Helminthiasis - diagnostic imaging ; Central Nervous System Helminthiasis - pathology ; Central Nervous System Helminthiasis - therapy ; Child ; Child, Preschool ; Echinococcosis - diagnostic imaging ; Echinococcosis - pathology ; Echinococcosis - therapy ; Female ; Follow-Up Studies ; Humans ; Hydatidosis ; Intracranial ; Male ; Medical sciences ; Middle Aged ; Neuroendoscopy ; Neurology ; Neurosurgery ; Neurosurgical Procedures ; Postoperative Complications - epidemiology ; Recurrence ; Retrospective Studies ; Spinal ; Spinal Cord - diagnostic imaging ; Spinal Cord - pathology ; Surgery (general aspects). 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-65c92280b12c847eaf331b63c4dd877df43e35d69be071dd9fe584a103ebf1023</citedby><cites>FETCH-LOGICAL-c511t-65c92280b12c847eaf331b63c4dd877df43e35d69be071dd9fe584a103ebf1023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22296522$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19781849$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Limaiem, Faten</creatorcontrib><creatorcontrib>Bellil, Selma</creatorcontrib><creatorcontrib>Bellil, Khadija</creatorcontrib><creatorcontrib>Chelly, Inès</creatorcontrib><creatorcontrib>Mekni, Amina</creatorcontrib><creatorcontrib>Khaldi, Moncef</creatorcontrib><creatorcontrib>Haouet, Slim</creatorcontrib><creatorcontrib>Zitouna, Moncef</creatorcontrib><creatorcontrib>Kchir, Nidhameddine</creatorcontrib><title>Primary hydatidosis of the central nervous system: A retrospective study of 39 Tunisian cases</title><title>Clinical neurology and neurosurgery</title><addtitle>Clin Neurol Neurosurg</addtitle><description>Abstract Objective To analyze epidemiological characteristics, clinical symptoms, radiological aspects, treatment and outcome of central nervous system hydatidosis and compare our results with those reported in literature. Patients and methods In our retrospective study, we reviewed 39 cases of primary central nervous system hydatid cysts operated on in our hospital between 1998 and 2007. Results There were 20 male and 19 female patients (sex-ratio M/F = 1.05) between 2 and 68 years of age (mean = 26.5 years). Thirteen of the patients were children (33.3%) with a mean age of 6.8 years and 26 were adults (66.7%) with a mean age of 36.3 years. The location of hydatid cysts was intracranial in 27 cases (69.2%) and spinal in 12 cases (30.8%). Headache and motor deficits were the predominant symptoms in patients with intracranial hydatidosis whereas back pain and spinal cord compression syndrome were the most frequent clinical presentations in patients with spinal hydatidosis. All patients underwent surgical resection of the cyst. Pathologic findings were consistent with hydatid cyst in all cases. During the follow-up period which ranged between 12 months and 5 years, 12 patients had recurrence (30.7%). Only one patient with intracranial hydatid cyst died postoperatively due to anaphylactic shock. Conclusion Despite all the advances in imaging techniques and therapeutic methods, central nervous system hydatidosis remains difficult to cure and patient outcomes are not satisfactory especially in case of spinal involvement due to the high incidence of recurrence.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - pathology</subject><subject>Central nervous system</subject><subject>Central Nervous System Helminthiasis - diagnostic imaging</subject><subject>Central Nervous System Helminthiasis - pathology</subject><subject>Central Nervous System Helminthiasis - therapy</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Echinococcosis - diagnostic imaging</subject><subject>Echinococcosis - pathology</subject><subject>Echinococcosis - therapy</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Hydatidosis</subject><subject>Intracranial</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neuroendoscopy</subject><subject>Neurology</subject><subject>Neurosurgery</subject><subject>Neurosurgical Procedures</subject><subject>Postoperative Complications - epidemiology</subject><subject>Recurrence</subject><subject>Retrospective Studies</subject><subject>Spinal</subject><subject>Spinal Cord - diagnostic imaging</subject><subject>Spinal Cord - pathology</subject><subject>Surgery (general aspects). 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Patients and methods In our retrospective study, we reviewed 39 cases of primary central nervous system hydatid cysts operated on in our hospital between 1998 and 2007. Results There were 20 male and 19 female patients (sex-ratio M/F = 1.05) between 2 and 68 years of age (mean = 26.5 years). Thirteen of the patients were children (33.3%) with a mean age of 6.8 years and 26 were adults (66.7%) with a mean age of 36.3 years. The location of hydatid cysts was intracranial in 27 cases (69.2%) and spinal in 12 cases (30.8%). Headache and motor deficits were the predominant symptoms in patients with intracranial hydatidosis whereas back pain and spinal cord compression syndrome were the most frequent clinical presentations in patients with spinal hydatidosis. All patients underwent surgical resection of the cyst. Pathologic findings were consistent with hydatid cyst in all cases. During the follow-up period which ranged between 12 months and 5 years, 12 patients had recurrence (30.7%). Only one patient with intracranial hydatid cyst died postoperatively due to anaphylactic shock. Conclusion Despite all the advances in imaging techniques and therapeutic methods, central nervous system hydatidosis remains difficult to cure and patient outcomes are not satisfactory especially in case of spinal involvement due to the high incidence of recurrence.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>19781849</pmid><doi>10.1016/j.clineuro.2009.09.001</doi><tpages>6</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Biological and medical sciences
Brain - diagnostic imaging
Brain - pathology
Central nervous system
Central Nervous System Helminthiasis - diagnostic imaging
Central Nervous System Helminthiasis - pathology
Central Nervous System Helminthiasis - therapy
Child
Child, Preschool
Echinococcosis - diagnostic imaging
Echinococcosis - pathology
Echinococcosis - therapy
Female
Follow-Up Studies
Humans
Hydatidosis
Intracranial
Male
Medical sciences
Middle Aged
Neuroendoscopy
Neurology
Neurosurgery
Neurosurgical Procedures
Postoperative Complications - epidemiology
Recurrence
Retrospective Studies
Spinal
Spinal Cord - diagnostic imaging
Spinal Cord - pathology
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Tomography, X-Ray Computed
Tunisia
Young Adult
title Primary hydatidosis of the central nervous system: A retrospective study of 39 Tunisian cases
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