<?xml version="1.0"?>
<Articles JournalTitle="Case Reports in Clinical Practice">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>2</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Monosymptomatic Manifestation of Clinically Isolated Syndrome with Sudden Sensory Neural Hearing Loss</title>
    <FirstPage>1</FirstPage>
    <LastPage>4</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mohammad reza</FirstName>
        <LastName>Najafi</LastName>
        <affiliation locale="en_US">Department of Neurology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Roshanak</FirstName>
        <LastName>Mehdipour-Dastjerdi</LastName>
        <affiliation locale="en_US">Department of Neurology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>04</Month>
        <Day>09</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>07</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Clinical presentation of demyelinating disorders is very heterogeneous, but&#xA0;initially isolated cranial nerve involvement, especially eighth nerve lesions,&#xA0;is extremely rare as the manifestation of clinically isolated syndrome (CIS)&#xA0;or multiple sclerosis (MS), so sudden sensory neural hearing loss (SNHL)&#xA0;is rarely a sole and presenting symptom of MS. A 31-year-old female&#xA0;presented with a history of left-sided ear fullness sensation and sudden&#xA0;hearing loss (without any history of trauma or infection); the pure-tone&#xA0;audiometry (PTA) showed unilateral SNHL pattern (high-frequency zone).&#xA0;The neurological and otolaryngologic examination was normal. Magnetic&#xA0;resonance imaging of the brain revealed several disseminated typical&#xA0;demyelinating plaques. The oligoclonal bands had been detected in the&#xA0;sample of cerebrospinal fluid. All of the routine laboratory data and serum&#xA0;autoantibodies were within normal ranges. Administration of high-dose&#xA0;corticosteroid improved her hearing. SNHL is a rare and atypical&#xA0;manifestation of CIS. Our case is assigned to be a high-risk CIS and may&#xA0;be developed to MS. It may be due to acute inflammatory demyelinating&#xA0;lesions of the cochlear nerve which could be a manifestation of CIS at first.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/112</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/112/64</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>2</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Perineural (Tarlov) Cyst Mimicking Lumbar Radiculopathy</title>
    <FirstPage>27</FirstPage>
    <LastPage>28</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mahdi</FirstName>
        <LastName>Safdarian</LastName>
        <affiliation locale="en_US">Department of Neurology, Hazrat Rasool Hospital, Iran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Sadra</FirstName>
        <LastName>Rohani</LastName>
        <affiliation locale="en_US">Department of Neurosurgery, Hazrat Rasool Hospital, Iran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Maryam</FirstName>
        <LastName>Zaribafian</LastName>
        <affiliation locale="en_US">Department of Neurology, Hazrat Rasool Hospital, Iran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Ghazal</FirstName>
        <LastName>Haeri</LastName>
        <affiliation locale="en_US">Department of Neurology, Hazrat Rasool Hospital, Iran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Rohani</LastName>
        <affiliation locale="en_US">Department of Neurology, Hazrat Rasool Hospital, Iran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>05</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>07</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">No Abstract</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/118</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/118/71</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>2</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">A 16-Year-Old Man with Vivax Malaria and Very Severe Thrombocytopenia</title>
    <FirstPage>5</FirstPage>
    <LastPage>8</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Fereshteh</FirstName>
        <LastName>Ghiasvand</LastName>
        <affiliation locale="en_US">Department of Infectious Diseases, School of Medicine, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Hamid</FirstName>
        <LastName>Emadi-Kuchak</LastName>
        <affiliation locale="en_US">Department of Infectious Diseases, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohamadreza</FirstName>
        <LastName>Salehi</LastName>
        <affiliation locale="en_US">Department of Infectious Diseases, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>01</Month>
        <Day>28</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Thrombocytopenia during the clinical course of Plasmodium falciparum&#xA0;malaria has been reported in different studies. However, for Plasmodium&#xA0;vivax malaria, profound thrombocytopenia (i.e., a platelet count below&#xA0;20,000/&#xB5;l), is infrequent. In this paper, we want to report of a case of vivax&#xA0;malaria with very severe thrombocytopenia. A 16-year-old man was&#xA0;examined in the emergency department because of fever, epistaxis, and&#xA0;very severe thrombocytopenia. In his phosphate-buffered saline evaluation,&#xA0;malaria vivax was confirmed. Artesunate because of severe malaria was&#xA0;begun. The fever was stopped after 24 hours. The last platelets count was&#xA0;185,000, and the patient was discharged with good condition. In&#xA0;conclusion, very severe thrombocytopenia as a complication of P. vivax&#xA0;malaria is rare; however, it may be manifested by the skin and mucous&#xA0;membrane bleeding and result in more severe complications, therefore&#xA0;prompt antimalarial treatment may lead to satisfactory outcome.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/102</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/102/65</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>2</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Uncommon Transmission of HIV Infection Due to a Criminal Knife Fight</title>
    <FirstPage>9</FirstPage>
    <LastPage>12</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Shahnaz</FirstName>
        <LastName>Sali</LastName>
        <affiliation locale="en_US">Infectious Diseases and Tropical Medicine Research Center AND Department of Infectious Diseases, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Simin Dokht</FirstName>
        <LastName>Shoaei</LastName>
        <affiliation locale="en_US">Department of Infectious Diseases, School of Medicine AND Clinical Research and Development Center, Imam Hossein Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Shabnam</FirstName>
        <LastName>Tehrani</LastName>
        <affiliation locale="en_US">Infectious Diseases and Tropical Medicine Research Center AND Department of Infectious Diseases, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>20</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Appropriate screening for HIV infection is the cornerstone of HIV-related&#xA0;care. Clinicians should be aware of criminalizing HIV exposure and&#xA0;transmission. We report a case of HIV-1 infection transmission caused by a&#xA0;knife fight between addicts and criminals. He was overlooked as an&#xA0;innocent victim and infected his wife without diagnosis. He was injured&#xA0;with a bloody knife used to damage a man minutes before. His 33-year-old&#xA0;wife was admitted with respiratory distress and responded to the treatment&#xA0;of pneumocystosis. In workup for predisposing factor of this opportunistic&#xA0;infection, AIDS was confirmed. The possible route of HIV-1 transmission&#xA0;was investigated and concluded most likely resulted sexually from his&#xA0;husband. Both of them have no behavioral risk factor for HIV infection.&#xA0;Peoples and physicians should be educated about epidemiology,&#xA0;transmission, and pre- and post-exposure prophylaxis of HIV.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/98</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/98/66</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>2</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Ventricular Tachyarrhythmia after Sildenafil Intake: A Case Report</title>
    <FirstPage>13</FirstPage>
    <LastPage>15</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Darush</FirstName>
        <LastName>Iranpoor</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, School of Medicine, Bushehr University of Medical Sciences, Bushehr, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>02</Month>
        <Day>25</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">This study reports the occurrence of ventricular tachyarrhythmia after&#xA0;sildenafil (Viagra&#xAE;) intake. A 60-year-old man was admitted to the hospital&#xA0;with ventricular arrhythmia after sildenafil (Viagra&#xAE;) intake. The&#xA0;echocardiography was normal, but in angiography, mild atherosclerotic&#xA0;plaques were seen. Comprehensive clinical trials are needed to prove any&#xA0;correlation between sildenafil intake and acute myocardial infarction.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/105</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/105/67</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>2</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Double Aortic Arch Anomaly Mimicking Asthma and Laryngomalacia: Two Case Reports</title>
    <FirstPage>16</FirstPage>
    <LastPage>20</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Tajdini</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Children&#x2019;s Medical Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mansoureh</FirstName>
        <LastName>Shariat</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Children&#x2019;s Medical Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammadreza</FirstName>
        <LastName>Mizaaghayan</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Children&#x2019;s Medical Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Sara</FirstName>
        <LastName>Memarian</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Children&#x2019;s Medical Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Parisa</FirstName>
        <LastName>Rahmani</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Children&#x2019;s Medical Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammadtaghi</FirstName>
        <LastName>Majnoon</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Children&#x2019;s Medical Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>03</Month>
        <Day>02</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">This report describes two patients (a 7-year-old boy and a 3-month-old boy)&#xA0;who have had chronic and recurrent respiratory distress and wheezing episodes&#xA0;since infancy. The elder one had been treated for hyper-reactive airway disease&#xA0;and asthma, and the other had been diagnosed with laryngomalacia. The&#xA0;problems had been associated with cyanosis and did not improve with routine&#xA0;treatment; therefore, we considered other underlying diseases, such as&#xA0;cardiovascular problems. The diagnostic workups revealed the &#x201C;double aortic&#xA0;arch&#x201D; which had not been diagnosed previously.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/106</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/106/68</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>2</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Nephrocutaneous Fistula: An Unusual Presentation of Xanthogranulomatous Pyelonephritis</title>
    <FirstPage>21</FirstPage>
    <LastPage>23</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Seyed Hassan</FirstName>
        <LastName>Inanloo</LastName>
        <affiliation locale="en_US">Department of Urology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Seyed Reza</FirstName>
        <LastName>Yahyazadeh</LastName>
        <affiliation locale="en_US">Department of Urology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Ali</FirstName>
        <LastName>Fallah</LastName>
        <affiliation locale="en_US">Department of Urology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>03</Month>
        <Day>09</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Spontaneous nephrocutaneous fistula is a rare manifestation of renal&#xA0;diseases. The majority of such fistulas are associated with&#xA0;xanthogranulomatous pyelonephritis, chronic renal tuberculosis,&#xA0;complicated renal stones, and post-traumatic or surgical injuries. We report&#xA0;the case of a 58-year-old male who presented with a history of massive&#xA0;lumbar cutaneous purulent discharge for 3 years. More investigations with&#xA0;ultrasonographic study and magnetic resonance imaging demonstrated the&#xA0;presence of a fistula between the kidney and skin. Detailed laboratory&#xA0;workup was negative for the diagnosis of renal tuberculosis. This patient&#xA0;was considered as a rare variant of xanthogranulomatous pyelonephritis&#xA0;and was managed effectively with a simple nephrectomy.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/108</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/108/69</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>2</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Difficult Temporary Pacing in a Patient with Interruption of Inferior Vena Cava and Hemiazygos/Accessory Hemiazygos Continuation</title>
    <FirstPage>24</FirstPage>
    <LastPage>26</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Reza</FirstName>
        <LastName>Hajizadeh</LastName>
        <affiliation locale="en_US">Cardiovascular Research Center AND Department of Cardiology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Bahram</FirstName>
        <LastName>Sohrabi</LastName>
        <affiliation locale="en_US">Cardiovascular Research Center AND Department of Cardiology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Fariborz</FirstName>
        <LastName>Akbarzadeh</LastName>
        <affiliation locale="en_US">Cardiovascular Research Center AND Department of Cardiology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Abdolmohammad</FirstName>
        <LastName>Ranjbar</LastName>
        <affiliation locale="en_US">Cardiovascular Research Center AND Department of Cardiology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>04</Month>
        <Day>07</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Many cardiovascular procedures such as temporary pacemaker insertion,&#xA0;electrophysiological studies, and percutaneous transmitral commissurotomy&#xA0;are carried through inferior vena cava (IVC). Its malformations such as its&#xA0;interruption with azygous/hemiazygous continuation, left-sided IVC, and&#xA0;double IVC can make some difficulties for cardiologists during these&#xA0;procedures. In this case report, we present the case of a 75-year-old male&#xA0;with recurrent episodes of syncope and bradycardia. Due to interrupted&#xA0;IVC, temporary pacing lead was difficultly advanced from the IVC to the&#xA0;accessory hemiazygos vein, left brachiocephalic vein, superior vena cava,&#xA0;right atrium, and right ventricle. Temporary pacemaker insertion is an&#xA0;invasive procedure and should be performed under the guidance of&#xA0;fluoroscopy. However, rarely, IVC malformations such as interrupted IVC&#xA0;make it difficult to do procedure in a short period of time. Rupture of IVC&#xA0;and some complications due to severe bradycardia can be prevented by&#xA0;understanding rare IVC malformations.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/110</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/110/70</pdf_url>
  </Article>
</Articles>
