<?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>4</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">A Rare Case of Acute Myeloblastc Leukemia With Blast Count Less Than 20% in Bone Marrow</title>
    <FirstPage>1</FirstPage>
    <LastPage>4</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Pardis</FirstName>
        <LastName>Nematollahi</LastName>
        <affiliation locale="en_US">Department of Hematopathology, Shiraz University of Medical Sciences, Shiraz, Iran, Department of Pathology, School of Medicine, Cancer Prevention Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Behnaz</FirstName>
        <LastName>Sabaghi</LastName>
        <affiliation locale="en_US">Department of Pathology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Alireza</FirstName>
        <LastName>Moafi</LastName>
        <affiliation locale="en_US">Department of Pediatric Hematology and Oncology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>08</Month>
        <Day>07</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2018</Year>
        <Month>12</Month>
        <Day>23</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">One of the diagnostic criteria for Acute Myeloblastic Leukemia (AML) is the presence of 20% myeloid blasts in peripheral blood or bone marrow. Some cases with recurrent cytogenetic abnormalities also fall in this category with blast cell count less than 20%. Thus, in the presence of these genetic abnormalities, the patients are classified as AML regardless of blast cell count. One of these genetic heterogeneities is t(8; 21) (q22, q22.1) which is more commonly seen in children and young adults. In this study, a 14-year-old boy is reported with a final diagnosis of AML, which was presented with fever and bicytopenia, clinically suspicious for acute leukemia. Laboratory results reported less than 20% blasts in bone marrow aspiration smears but genetic alteration t(8; 21) (q22, q22.1) was detected by molecular exams.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/210</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/210/287</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>4</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Tense Ascites as a Presentaton of Protein S Defciency in a 9-Year-Old Boy</title>
    <FirstPage>5</FirstPage>
    <LastPage>8</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Masoumeh</FirstName>
        <LastName>Asgarshirazi</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mehrnoush</FirstName>
        <LastName>Ghafarypour</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Yahya</FirstName>
        <LastName>Aghighi</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Seyyedreza</FirstName>
        <LastName>Raeeskarami</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mehri</FirstName>
        <LastName>Najafi</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>09</Month>
        <Day>13</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>01</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Ascites is not a usual finding in prehepatic portal hypertension, including portal vein thrombosis, but when portal vein thrombosis is acute and massive, ascites can be a presenting feature. We report a 9-year-old boy with tense ascites and portal and superior mesenteric vein thrombosis. A 9-year-old boy was evaluated for tense ascites which led to umbilical hernia since one month before admission. He did not have any clinical or laboratory stigmata of parenchymal liver disease. Imaging studies showed superior mesenteric and portal vein thrombosis. In laboratory tests for pre-thrombotic states, he suffered from significant protein S deficiency. Thrombophilic states like protein S deficiency predispose patient to vascular thrombosis. This vascular thrombosis can be present with signs and symptoms related to their territories. Prevention of thrombosis and rethrombosis with anticoagulant therapy is recommended.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/220</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/220/288</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>4</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Azathioprine-Induced Severe Bone Marrow Suppression</title>
    <FirstPage>9</FirstPage>
    <LastPage>13</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Marzie</FirstName>
        <LastName>Ghalamkari</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Cancer Institute, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Sahar</FirstName>
        <LastName>Karimpour Reihan</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Nasim</FirstName>
        <LastName>Khajavi Rad</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mahsa</FirstName>
        <LastName>Abbaszadeh</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>10</Month>
        <Day>27</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>01</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Aplastic anemia is characterized by bone marrow failure and pancytopenia. It could be due to autoimmune disorders, radiation, drugs, or chemicals. Drugs that mostly cause aplastic anemia include chloramphenicol, non-steroidal anti-inflammatory drugs, antiepileptic drugs, gold salts, and antithyroid drugs. Clinical sign and symptoms often result from pancytopenia that includes signs of anemia and bleeding. In some patients, fever and sepsis are seen that are due to neutropenia. Azathioprine is a purine antimetabolite, an immunosuppressive drug that causes myelosuppression and pancytopenia, especially in patients who have some degrees of TPMT (Thiopurine Methyltransferase) activity. We present a patient who admitted to our hospital with fever and pancytopenia and a history of recent azathioprine treatment. Because of delay in the recovery of pancytopenia, she was suspected of aplastic anemia, and bone marrow aspiration and biopsy were done for her.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/231</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/231/289</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>4</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Traumatc Herniaton of the Buccal Fat Pad</title>
    <FirstPage>14</FirstPage>
    <LastPage>16</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Reza</FirstName>
        <LastName>Erfanian</LastName>
        <affiliation locale="en_US">Otolaryngology Head and Neck Research Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Saeed</FirstName>
        <LastName>Shakiba</LastName>
        <affiliation locale="en_US">Department of Otolaryngology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Sadeq</FirstName>
        <LastName>Najafi</LastName>
        <affiliation locale="en_US">Department of Otolaryngology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Saeed</FirstName>
        <LastName>Sohrabpour</LastName>
        <affiliation locale="en_US">Otolaryngology Head and Neck Research Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>10</Month>
        <Day>30</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>01</Month>
        <Day>21</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Buccal Fat Pad is an encapsulated mass of adipose tissue located within the buccal facial spaces, between the buccinator and masseter muscles. Intraoral traumatic herniation of Buccal Fat Pad, often seen in young children, has been reported as a rare case. In this report, we present a case of traumatic Buccal Fat Pad herniation which at first was misdiagnosed as a malignant tumor.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/232</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/232/290</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>4</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Primary Echinococcal Synovits</title>
    <FirstPage>17</FirstPage>
    <LastPage>19</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mahnaz</FirstName>
        <LastName>Pejman Sani</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mahbube</FirstName>
        <LastName>Ebrahimpur</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mahnaz</FirstName>
        <LastName>Torki</LastName>
        <affiliation locale="en_US">Department of Infectious Diseases, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Neda</FirstName>
        <LastName>Alijani</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran, Department of Infectious Diseases, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>11</Month>
        <Day>07</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>01</Month>
        <Day>22</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Hydatid cyst is a parasitic infection caused by the larvae of Echinococcus granulosus. We report a rare case of primary echinococcal synovitis in a 37-year-old woman who was referred to our clinic with pain and swelling of the right knee.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/234</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/234/291</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>4</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">A Rare Case of Hypoglycemic Unawareness in a Patent With Chronic Congestve Heart Failure</title>
    <FirstPage>20</FirstPage>
    <LastPage>22</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Yawar</FirstName>
        <LastName>Yaseen</LastName>
        <affiliation locale="en_US">Directorate of Health Services, Kashmir, Jammu and Kashmir, India.</affiliation>
      </Author>
      <Author>
        <FirstName>Parvaiz</FirstName>
        <LastName>Shah</LastName>
        <affiliation locale="en_US">Department of Medicine, Government Medical College, Srinagar, Jammu and Kashmir, India.</affiliation>
      </Author>
      <Author>
        <FirstName>Irfan</FirstName>
        <LastName>Mir</LastName>
        <affiliation locale="en_US">Government Medical College, Srinagar, Jammu and Kashmir, India.</affiliation>
      </Author>
      <Author>
        <FirstName>Saika</FirstName>
        <LastName>Amreen</LastName>
        <affiliation locale="en_US">Department of Radio Diagnosis, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, Jammu and Kashmir, India.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>11</Month>
        <Day>28</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>01</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Hypoglycemia and hypoglycemic unawareness is usually a complication of tight glycemic control in insulin-dependent diabetes mellitus. To our knowledge, this is the first case report of hypoglycemic unawareness subsequent to cardiac failure induced hypoglycemia of prolonged duration. Through this case report, we aimed to highlight that hypoglycemia should be suspected as a cause of decreased level of consciousness in patients suffering from recurrent congestive cardiac failure , as it can be easily overlooked and the condition can easily be reversed by simply administering adequate glucose.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/240</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/240/292</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>4</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Tracheobronchopathia Osteochondroplastca</title>
    <FirstPage>23</FirstPage>
    <LastPage>26</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Ehsan</FirstName>
        <LastName>Sanaei</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Fathemeh</FirstName>
        <LastName>Aghaei Meybodi</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Marzie</FirstName>
        <LastName>Vaghefi</LastName>
        <affiliation locale="en_US">Department of Pediatrics, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>11</Month>
        <Day>29</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>01</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Tracheobronchopathia Osteochondroplastica (TPO) is a rare benign disorder of the lower part of the trachea and the upper part of the main bronchi. A 55-year-old female patient had been referring to our pulmonary and critical care center suffering from chronic dry cough and breathlessness on exertion and retrosternal pain for several months who was admitted to our center when she was complaining about breathlessness on exertion and chronic dry cough and retrosternal pain.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/241</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/241/293</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>4</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Many Segments in Neutrophils of a Patent With Megaloblastc Anemia</title>
    <FirstPage>27</FirstPage>
    <LastPage>28</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Sahar</FirstName>
        <LastName>Karimpour Reyhan</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mahsa</FirstName>
        <LastName>Abbaszadeh</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Nasim</FirstName>
        <LastName>Khajavi Rad</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>10</Month>
        <Day>26</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2018</Year>
        <Month>12</Month>
        <Day>17</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">No Abstract###
&#xD;

&#xA0;</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/230</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/230/294</pdf_url>
  </Article>
</Articles>
