<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Medical Journal of the Islamic Republic Of Iran</title>
<title_fa>مجله پزشکی جمهوری اسلامی ایران</title_fa>
<short_title>Med J Islam Repub Iran</short_title>
<subject>Medical Sciences</subject>
<web_url>http://mjiri.iums.ac.ir</web_url>
<journal_hbi_system_id>2</journal_hbi_system_id>
<journal_hbi_system_user>journal2</journal_hbi_system_user>
<journal_id_issn>1016-1430</journal_id_issn>
<journal_id_issn_online>2251-6840</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>10.18869/mjiri</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1381</year>
	<month>2</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2002</year>
	<month>5</month>
	<day>1</day>
</pubdate>
<volume>16</volume>
<number>1</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>AUTOERYTHROCYTE SENSITIZATION SYNDROME: REPORT OF A CASE AND REVIEW OF THE LITERATURE</title>
	<subject_fa>Dermatology</subject_fa>
	<subject>Dermatology</subject>
	<content_type_fa>case report</content_type_fa>
	<content_type>case report</content_type>
	<abstract_fa></abstract_fa>
	<abstract>Autoerythrocyte sensitization syndrome CABS) is a rare purpuric disorder of
women characterized by inflammatory and painful ecchymotic lesions unrelated
to blood clotting or vascular abnormalities. Gastrointestinal bleeding, hematuria,
headache or syncopal attacks may also be observed.
Our patient is a 33-year-old woman presenting with recurrent severe painful
ecchymotic lesions on both lower extremities associated with headache, palpitation
and weakness. The diagnosis of AES was confirmed by skin testing with
autologous washed red blood cells. No internal bleeding was detected. She was
treated with vitamin C with some success.

</abstract>
	<keyword_fa></keyword_fa>
	<keyword>AES, Gardner-Diamond Syndrome, Painful Bruising Syndrome, Psychogenic Purpura</keyword>
	<start_page>51</start_page>
	<end_page>53</end_page>
	<web_url>http://mjiri.iums.ac.ir/browse.php?a_code=A-10-298-232&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>L</first_name>
	<middle_name></middle_name>
	<last_name>DASTGHEIB</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>20031947532846006811</code>
	<orcid>20031947532846006811</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>From the Departments of Dermatology and Pathology, Shiraz University of Medical Sciences, Shiraz, I.R. Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>P</first_name>
	<middle_name></middle_name>
	<last_name>PEYRAVI</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>20031947532846006812</code>
	<orcid>20031947532846006812</orcid>
	<coreauthor>No</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>FS</first_name>
	<middle_name></middle_name>
	<last_name>ASLANI</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>20031947532846006813</code>
	<orcid>20031947532846006813</orcid>
	<coreauthor>No</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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