<?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>8</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2023</Year>
        <Month>07</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Plasma Therapy for Medication-Related Osteonecrosis of the Jaws- A Case Report</title>
    <FirstPage>1</FirstPage>
    <LastPage>4</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Maryam</FirstName>
        <LastName>Jalili Sadrabad</LastName>
        <affiliation locale="en_US">Oral and Maxillofacial Medicine Department, Dental School, Semnan University of Medical Science, Semnan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Elham</FirstName>
        <LastName>Saberian</LastName>
        <affiliation locale="en_US">PhD and research student, Pavol Jozef &#x160;af&#xE1;rik University, Klinika Bacikova, Ko&#x161;ice, Slovakia.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2022</Year>
        <Month>05</Month>
        <Day>08</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2022</Year>
        <Month>12</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Medication-related osteonecrosis of the jaw (MRONJ) is a side effect of anti-bone resorption medications. Nowadays antiresorptive medications like bisphosphonate and monoclonal antibodies like denosumab that have been prescribed for bone disorders and metastatic cancer are becoming increasingly common. Although these medications are quite efficient at reducing bone resorption, they can develop osteomyelitis and jaw necrosis as a side effect. A 65-year-old woman was referred to the Oral Medicine Department of Semnan University of Medical Sciences with diffuse bilateral mandibular osteonecrosis, with a history of osteopetrosis and under-treatment of bisphosphonate. This complication started after tooth extraction and without any healing 5 years ago. After 3 sessions of plasma therapy, obvious improvement was seen. A proper medical history and a routine oral examination before treating with any invasive dental treatment are necessary to avoid any medication-related osteonecrosis of the jaw or mucosal abnormalities.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/687</web_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>8</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2023</Year>
        <Month>07</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Pulmonary Artery Aneurysm Dilemma in Pregnancy: A Case Report</title>
    <FirstPage>5</FirstPage>
    <LastPage>8</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Shadi</FirstName>
        <LastName>Zamansaraei</LastName>
        <affiliation locale="en_US">Department of Gynecology Surgery, Isfahan University of medical Sciences, Isfahan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Milad</FirstName>
        <LastName>Nazari Sabet</LastName>
        <affiliation locale="en_US">Resident of General Surgery, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Parvin</FirstName>
        <LastName>Bahrami</LastName>
        <affiliation locale="en_US">Department of Cardiology, Alzahra University Hospital, Isfahan University of Medical Science, Isfahan, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2022</Year>
        <Month>07</Month>
        <Day>06</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2023</Year>
        <Month>02</Month>
        <Day>12</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Pulmonary Artery Aneurysm (PAA), defined as greater than 40 mm dilation of the main pulmonary artery wall, in female and above 43 mm in males is a rare and fatal defect. Since there is a high risk for rupture, especially in cases of symptomatic or severe dilatation, surgical intervention is suggested. There is no recommendation about therapeutic methods based on the diameter of the pulmonary aneurysm in pregnancy in
the guidelines. In this rare and unique report, we described a 26-year-old pregnant woman with previous history of biologic pulmonary valve replacement referred to the joint clinic of heart disease and pregnancy at 15 weeks of pregnancy because transthoracic echocardiography showed an aneurysm of the main pulmonary artery (55mm). Due to pulmonary artery diameter and risk of dissection, we informed her about the risks and
recommended therapeutic abortion, but she refused and, fortunately no complication occurred during close observation in pregnancy and few months later. There is no specific recommendation about therapeutic methods based on the diameter of the pulmonary aneurysm in pregnancy in the guidelines, but referring to
the aortic aneurysm guidelines recommendation, pregnancy termination when PA diameter &gt; 5.5 cm because of the higher risk of dissection. Other factors should be considered to determine the risk of dissection in pregnancy include; categorized PA aneurysms to high or low intravascular PA pressure, PA diameter growth rate, and causative mechanisms. Thus, if pregnancy occurs, decisions about each patient will vary depending on risk factors</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/709</web_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>8</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2023</Year>
        <Month>07</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Post-Cardiac Injury Syndrome (Dressler Syndrome) Following Atrial Septal Defect (ASD) Repair: A Case Report</title>
    <FirstPage>9</FirstPage>
    <LastPage>13</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Ali</FirstName>
        <LastName>Mirabi</LastName>
        <affiliation locale="en_US">Resident of Cardiology, Clinical Research and Development center, Shahid Beheshti Hospital, Qom University of Medical Sciences, Qom, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Reihane</FirstName>
        <LastName>Tabaraii</LastName>
        <affiliation locale="en_US">Clinical Research and Development Center, Shahid Beheshti Hospital, Qom University of Medical Sciences, Qom, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Morteza</FirstName>
        <LastName>Sedaqat</LastName>
        <affiliation locale="en_US">Medical Student, Student Research Committee, Qom University of Medical Sciences, Qom, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Saba</FirstName>
        <LastName>Gaeini</LastName>
        <affiliation locale="en_US">Medical Student, Student Research Committee, Qom University of Medical Sciences, Qom, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Maryam</FirstName>
        <LastName>Masoumi</LastName>
        <affiliation locale="en_US">Clinical Research and Development Center, Shahid Beheshti Hospital, Qom University of Medical Sciences, Qom, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2022</Year>
        <Month>04</Month>
        <Day>19</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2023</Year>
        <Month>04</Month>
        <Day>26</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Dressler syndrome is a type of secondary pericarditis that can be accompanied by pleural effusion or pericardial effusion resulting from injury of the pericardium or heart tissue. A 33-year-old male was admitted to the emergency department with pleuritic chest pain radiating to both shoulders and fever. Two months before the admission, the patient underwent traditional open-heart surgery with median sternotomy and pericardiectomy for atrial septal defect (ASD) closure. Blood tests showed elevated acute phase reactants (leukocytosis, high erythrocyte sedimentation rate, and C-reactive protein). Left-sided pleural effusion was revealed on chest CT scan. Diagnosis of Dressler syndrome was established. The patient&#x2019;s pleuritic chest pain and shoulder pain improved clinically with a short course of colchicine. Although Dressler syndrome is rarely seen, it should be considered in the differential diagnosis of pleuritic chest pain. Special attention should be paid to Dressler&#x2019;s syndrome because pericarditis can develop following cardiac surgery</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/677</web_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>8</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2023</Year>
        <Month>07</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Biliary Ascariasis with Gallbladder Invasion: A Unique Entity</title>
    <FirstPage>14</FirstPage>
    <LastPage>15</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Manzoor</FirstName>
        <LastName>Hussain</LastName>
        <affiliation locale="en_US">Senior Resident, Department of Radiology, SKIMS SOURA, J&amp;K, INDIA.</affiliation>
      </Author>
      <Author>
        <FirstName>Nargis</FirstName>
        <LastName>Banoo</LastName>
        <affiliation locale="en_US">Senior Resident, Department of Paediatrics, GMC srinagar, J&amp;K, INDIA.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2022</Year>
        <Month>06</Month>
        <Day>16</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2023</Year>
        <Month>02</Month>
        <Day>12</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Intestinal Ascariasis is a common helminthic infection in developing countries and in some rare cases, worms migrate to the biliary tract and gall bladder. Extraintestinal biliary ascariasis presents with jaundice, right upper quadrant abdominal pain, and vomiting. Ultrasonography is a useful diagnostic modality. Albendazole and Mebendazole are commonly used anti-helmintic agents for conservative management, whereas endoscopic removal is needed in rare cases.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/702</web_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>8</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2023</Year>
        <Month>07</Month>
        <Day>22</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Severe Diabetic Ketoacidosis and Coronavirus 2019 (COVID-19) Infection led to Diagnosis of Autoimmune Polyglandular Syndrome</title>
    <FirstPage>16</FirstPage>
    <LastPage>20</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Meraj</FirstName>
        <LastName>Tavakoli</LastName>
        <affiliation locale="en_US">Endocrinology and Metabolism Research Center (EMRC), Vali-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Soghra</FirstName>
        <LastName>Rabizadeh</LastName>
        <affiliation locale="en_US">Endocrinology and Metabolism Research Center (EMRC), Vali-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Sara</FirstName>
        <LastName>Seifouri</LastName>
        <affiliation locale="en_US">Endocrinology and Metabolism Research Center (EMRC), Vali-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Alireza</FirstName>
        <LastName>Esteghamati</LastName>
        <affiliation locale="en_US">Endocrinology and Metabolism Research Center (EMRC), Vali-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Manouchehr</FirstName>
        <LastName>Nakhjavani</LastName>
        <affiliation locale="en_US">Endocrinology and Metabolism Research Center (EMRC), Vali-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2022</Year>
        <Month>05</Month>
        <Day>19</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2022</Year>
        <Month>12</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">To this day, millions of people in the world have been diagnosed with corona virus 2019 (COVID-19). This disease cannot only lead to higher mortality rates among those&#xA0;with underlying Diabetes Mellitus (DM), but also may trigger DM in susceptible patients. Therefore, incidence of new-onset DM increased during the pandemic as a result; treatment of patients with diabetes and COVID-19 is important and needs further investigations. Here, we report a 27-year- old woman with past medical history of premature ovarian failure (POF) since14 years ago, who initially presented with severe diabetic ketoacidosis (DKA) which was triggered by COVID-19 and later through her lab results hypoparathyroidism was also detected. She was treated for DKA and COVID-19 Infection concomitantly, and she was also diagnosed with autoimmune polyglandular syndrome due to her multiple autoimmune endocrine organ involvements.&#xA0;</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/688</web_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>8</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2023</Year>
        <Month>07</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Acute Esophageal Necrosis as a Result of Taking Herbal Medicine</title>
    <FirstPage>21</FirstPage>
    <LastPage>23</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Narjes</FirstName>
        <LastName>Zarei Jalalabadi</LastName>
        <affiliation locale="en_US">Department Internal medicine, Imam Khomeini Hospital complexs,Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Nasim</FirstName>
        <LastName>Khajavirad</LastName>
        <affiliation locale="en_US">Department Internal medicine, Imam Khomeini Hospital complexs,Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Samaneh</FirstName>
        <LastName>Parsa</LastName>
        <affiliation locale="en_US">Department Internal medicine, Imam Khomeini Hospital complexs,Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Sahar</FirstName>
        <LastName>Karimpour Reyhan</LastName>
        <affiliation locale="en_US">Department Internal medicine, Imam Khomeini Hospital complexs,Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>10</Month>
        <Day>31</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2023</Year>
        <Month>02</Month>
        <Day>12</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Nowadays People use herbal medicines to try to maintain or improve their health but sometimes they cause side-effects and some herbal drug may also interact with medication. We reported a 37 -year-old man who presented to the emergency department with sever watery diarrhea, vomiting, dysphagia, bicytopenia, renal failure and Acute esophageal necrosis, also known as black esophagus which is a rare syndrome characterized by a striking diffuse circumferential black appearance of the esophageal mucosa that universally affects the distal esophagus, 2-days after use of herbal drug named suranjan. Suranjan is a herbal formulation used to treat Rheumatoid arthritis.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/615</web_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>8</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2023</Year>
        <Month>07</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Right Lower Extremity Numbness- an Atypical Presentation of Acute Aortic Dissection</title>
    <FirstPage>24</FirstPage>
    <LastPage>28</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>Masoumi</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Qom University of Medical Sciences, Qom, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Seyed Mojtaba</FirstName>
        <LastName>Alavi</LastName>
        <affiliation locale="en_US">Student Research Committee, Qom University of Medical Sciences, Qom, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Morteza</FirstName>
        <LastName>Sedaqat</LastName>
        <affiliation locale="en_US">Student Research Committee, Qom University of Medical Sciences, Qom, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Shahidi</LastName>
        <affiliation locale="en_US">Department of Emergency Medicine, Qom University of Medical Sciences, Qom, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2022</Year>
        <Month>10</Month>
        <Day>09</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2023</Year>
        <Month>02</Month>
        <Day>22</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Acute aortic dissection (AAD) is one of the most challenging and emergency conditions in the health care system. It`s associated with high mortality. A 55-year-old person was admitted to the emergency department due to numbness of his right leg. The patient had no complaints of chest pain on arrival. However, echocardiography revealed aortic dissection and computed tomography (CT) scan confirmed the diagnosis. The patient was immediately referred to Rajaei hospital for further specialized procedures. He went into the operating room directly and had a successful operation of aortic dissection repair. Rarely AAD has atypical manifestation and may have unusual clinical presentations. Thus, it could cause a delay in establishment of diagnosis of this emergent condition. The purpose of this report was to introduce a rare initial presentation of an atypical aortic dissection.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/742</web_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>8</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2023</Year>
        <Month>07</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Spontaneous Transformation of Intramural Myoma into Peduncle During Cesarean Section in a 33-year Woman: A Case Report</title>
    <FirstPage>29</FirstPage>
    <LastPage>33</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>Yazdi</LastName>
        <affiliation locale="en_US">Department of Obstetrics and Gynecology, School of Medicine, Nekouei-Hedayati-Forghani Hospital, Qom University of Medical Sciences, Qom, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Seyed Mohammad Hashem</FirstName>
        <LastName>Montazeri</LastName>
        <affiliation locale="en_US">Student Research Committee, School of Medicine, Qom University of Medical Sciences, Qom, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2022</Year>
        <Month>04</Month>
        <Day>15</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2022</Year>
        <Month>12</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">We report a 33 years multipara pregnant woman who presented with vaginal bleeding due to intramural myoma and preeclampsia. After cesarean section, the myoma changed to the peduncle type and entered the internal space from the inner thickness of the uterus. This infrequent phenomenon made it easier to operate and remove the myoma within a few hours after the cesarean section. Finally, the mother and baby were discharged from the hospital safely after a few days.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/674</web_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>8</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2023</Year>
        <Month>07</Month>
        <Day>22</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">A Case of Antenatal Diagnosis of Ectopia Cordis with Cardiac Disease</title>
    <FirstPage>34</FirstPage>
    <LastPage>38</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Fariba</FirstName>
        <LastName>Rashidighader</LastName>
        <affiliation locale="en_US">Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammadrafie</FirstName>
        <LastName>Khorgami</LastName>
        <affiliation locale="en_US">Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Elio</FirstName>
        <LastName>Caruso</LastName>
        <affiliation locale="en_US">Department of Pediatric Cardiology,Mediterranean Pediatric Cardiology Center "Bambin Ges&#xF9;", San Vincenzo Hospital, Taormina, Italy.</affiliation>
      </Author>
      <Author>
        <FirstName>Farruggio</FirstName>
        <LastName>Silvia</LastName>
        <affiliation locale="en_US">Department of Pediatric Cardiology,Mediterranean Pediatric Cardiology Center "Bambin Ges&#xF9;", San Vincenzo Hospital, Taormina, Italy.</affiliation>
      </Author>
      <Author>
        <FirstName>Reza</FirstName>
        <LastName>Masihi</LastName>
        <affiliation locale="en_US">Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2022</Year>
        <Month>10</Month>
        <Day>27</Day>
      </PubDate>
    ical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Faeze</FirstName>
        <LastName>Salahshour</LastName>
        <affiliation locale="en_US">Department  of  Radiology,  Advanced  Diagnostic  and  Interventional  Radiology  Research  Centre  (ADIR),  IKHC,  Tehran  University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mahdi</FirstName>
        <LastName>Zangi</LastName>
        <affiliation locale="en_US">PhD Candidate, University of Otago, Christchurch, New Zealand.</affiliation>
      </Author>
      <Author>
        <FirstName>Somayeh</FirstName>
        <LastName>Mirbagheri</LastName>
        <affiliation locale="en_US">Emergency medicine resident, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Eftekhari</LastName>
        <affiliation locale="en_US">Assistant Professor, Emergency Medicine Department, Tehran University of Medical Sciences, Keshavarz Blvd., Tehran,  Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2023</Year>
        <Month>10</Month>
        <Day>04</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>02</Month>
        <Day>26</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">The abdomen is the second most common site for sepsis. This potentially life- threatening condition necessitates finding the source and providing prompt medical and/or surgical treatment. This presentation reveals an uncommon cause of intra- abdominal sepsis.A 43-year-old woman presented to the emergency department with abdominal pain, tachycardia, tachypnea, and generalized abdominal tenderness. The evaluation of the laboratory tests showed an elevation in white blood cell count and liver enzymes. Ultrasonography of the liver revealed the presence of hydatid cysts, and the abdomino- pelvic computed tomography scan with contrast displayed multiple pyogenic cysts in her liver, one of which had ruptured into the peritoneum. She underwent surgery, received antimicrobial agents, and was successfully discharged without experiencing any complications.One clinical presentation of a hepatic hydatid cyst could be intra-abdominal sepsis, which requires emergency surgery along with antibiotic and anti-helminthic drugs.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/877</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/877/594</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>8</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2024</Year>
        <Month>09</Month>
        <Day>29</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Complicated Progress of Granulomatosis with  Polyangiitis - A Case Presentation And Review of  literature</title>
    <FirstPage>270</FirstPage>
    <LastPage>274</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Matineh Sadat</FirstName>
        <LastName>Tabatabaei</LastName>
        <affiliation locale="en_US">School of Nursing and Midwifery, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mostafa</FirstName>
        <LastName>Mortazi</LastName>
        <affiliation locale="en_US">Faculty of Medicine, Alborz University of Medical Sciences, Alborz, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2023</Year>
        <Month>12</Month>
        <Day>03</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>05</Month>
        <Day>05</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Granulomatosis with polyangiitis, previously known as Wegener&#x2019;s, is a necrotizing vascular disease that affects small blood vessels and may cause damage to the respiratory tract and kidneys. In this article, we report on a 50-year-old male with a complicated disease process who experienced rare bladder and renal complications and several adverse drug reactions. Despite using drug alternatives, the side effects remained mostly the same. Therefore, by studying different cases and articles, we establish the relation between these findings and the specifications of granulomatosis with polyangiitis. This case underscores the complexity of managing this condition and the need for personalized treatment strategies.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/901</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/901/595</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>8</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2024</Year>
        <Month>09</Month>
        <Day>29</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Cesarean Scar Choriocarcinoma Following a Cesarean  Scar Molar Pregnancy: A Case Report</title>
    <FirstPage>275</FirstPage>
    <LastPage>280</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Azadeh</FirstName>
        <LastName>Tarafdari</LastName>
        <affiliation locale="en_US">Department of Obstetrics and Gynecology, Imam Khomeini Hospital Complex, Vali-e-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Sanaz</FirstName>
        <LastName>Ghashghaee</LastName>
        <affiliation locale="en_US">Department of Obstetrics and Gynecology, Imam Khomeini Hospital Complex, Vali-e-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zeinab</FirstName>
        <LastName>Mansouri</LastName>
        <affiliation locale="en_US">Department of Obstetrics and Gynecology, Imam Khomeini Hospital Complex, Vali-e-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammadamin</FirstName>
        <LastName>Parsaei</LastName>
        <affiliation locale="en_US">Maternal, Fetal &amp; Neonatal Research Center, Family Health Research Institute, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>01</Month>
        <Day>15</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>05</Month>
        <Day>05</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Gestational choriocarcinoma, a rare variant of gestational trophoblastic disease, typically arises from abnormal trophoblastic cell proliferation post-pregnancy, often associated with a hydatidiform mole. While most choriocarcinoma cases develop within the uterine cavity, an exceedingly rare manifestation occurs within a previous cesarean section scar. In our study, a 31-year-old woman with a history of hydatidiform mole presented with amenorrhea and spotting. Initial assessments revealed elevated beta-human chorionic gonadotropin (&#x3B2;hCG) levels and a heteroechoic mass at her prior cesarean section scar in sonographic examination. Histopathologic findings and the metastatic workup categorized the patient as FIGO stage I, indicating no metastasis. Due to the absence of metastasis, adjuvant chemotherapy was omitted. Total abdominal hysterectomy confirmed choriocarcinoma. Post-surgery, &#x3B2;hCG levels notably decreased, remaining negative during the two-year follow-up with no reported symptoms. Our findings suggest that surgical resection and meticulous &#x3B2;hCG monitoring may be a promising treatment strategy for non-metastatic choriocarcinoma.</abstract>
    <web_url>https://crcp.tums.ac.ir/index.php/crcp/article/view/918</web_url>
    <pdf_url>https://crcp.tums.ac.ir/index.php/crcp/article/download/918/596</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Case Reports in Clinical Practice</JournalTitle>
      <Issn>2538-2683</Issn>
      <Volume>8</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2024</Year>
        <Month>09</Month>
        <Day>29</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Airbag Deployment And Tinnitus Emergence Following  Car Crash, a Case Report And a Brief Literature Review</title>
    <FirstPage>281</FirstPage>
    <LastPage>283</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Hossein Azizi</LastName>
        <affiliation locale="en_US">Associate Professor of Otolaryngology, Academy of Medical Sciences of the I.R. of Iran, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Frough</FirstName>
        <LastName>Aghanejad</LastName>
        <affiliation locale="en_US">Audiologist, Tehran, Iran</affili