<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Tehran University Medical Journal</title>
<title_fa>مجله دانشکده پزشکی، دانشگاه علوم پزشکی تهران</title_fa>
<short_title>Tehran Univ Med J</short_title>
<subject>Medical Sciences</subject>
<web_url>http://tumj.tums.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>1683-1764</journal_id_issn>
<journal_id_issn_online>1735-7322</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.18869/acadpub.tumj</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>000</journal_id_sid>
<journal_id_nlai>000</journal_id_nlai>
<journal_id_science>000</journal_id_science>
<language>fa</language>
<pubdate>
	<type>jalali</type>
	<year>1380</year>
	<month>2</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2001</year>
	<month>5</month>
	<day>1</day>
</pubdate>
<volume>59</volume>
<number>2</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>fa</language>
	<article_id_doi></article_id_doi>
	<title_fa>معرفی یک بیمار مبتلا به Giant cell tumor استخوان کشکک همراه با متاستازی ریوی</title_fa>
	<title>The Susac&#039;s syndrome: A case report from neurology ward of Imam Khomeiny Hospital, 1999</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa>استخوان کشکک محل شایعی برای تومورهای اولیه استخوان نمی باشد و غالب این تومورها به صورت موردی گزارش شده اند ولی Giant cell tumor یکی از تومورهای شایع استخوان کشکک محسوب می شود. در مقاله حاضر ضمن بررسی یک بیمار مبتلا به Giant cell tumor این استخوان که همراه با متاستازهای متعدد ریوی بوده، راجع به این مقوله بررسی بیشتری صورت گرفته است.&lt;/p&gt;                                                                  &lt;/span&gt;</abstract_fa>
	<abstract>This syndrome is a very rare neurological presentation which was first reported by Susac in 1975, and usually involves the young women with triad of: (1) Visual loss due to occlusion of retinal artery branches. (2) Subacute encephalopathy with psychic manifestation, personality disorders, involvement of the cortico-spianal tracts, pseudo-bulbar, focal or generalized seizures and myoclonic jerks. (3) Bilateral sensory neural hearing loss with tinnitus. All of the symptoms and signs are pathologically due to microinfarcts. It&#039;s pathogenesis is unknown. Brain biopsy shows multiple microinfarctions. Diagnosis of this syndrome is based on the clinical tiard, retinal angiography and neuroimaging studies. In this report, a young lady of 25 years old was referred to neurology ward of Imam Khomeini Hospital with above mentioned symptoms an signes and was recognized as a case of this syndrome.</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Susac!@#$%s syndrome,Subacute encephalopathy,Personality disorders</keyword>
	<start_page>1</start_page>
	<end_page>5</end_page>
	<web_url>http://tumj.tums.ac.ir/browse.php?a_code=A-10-25-1334&amp;slc_lang=fa&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name></first_name>
	<middle_name></middle_name>
	<last_name>Ghlich Nia Omrani H</last_name>
	<suffix></suffix>
	<first_name_fa>محمود</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>معتمدی</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name></first_name>
	<middle_name></middle_name>
	<last_name>Ghaffar Poor M</last_name>
	<suffix></suffix>
	<first_name_fa>رامین</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>اسپندار</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
