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Volume 39(1); January 2016

Case Reports
[English]
Acute Fulminant Myocarditis Recovered from Electro-Mechanical Dissociation in Scrub Typhus
Young Hak Jung, Minjoo Lee, Kyoung Hwa Lee, Ji Hoon Lee, Seok-hyung Kim, Byoung Kwon Lee
Ewha Med J 2016;39(1):1-5.   Published online January 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.1.1

Scrub typhus, caused by Orientia tsutsugamushi, is an acute febrile illness. Characteristics of tsutsugamushi disease are fever, rash and eschar. However, severe complications might rarely occur, such as acute fulminant myocarditis caused by scrub typhus. Thus, there are few reports of recovery from seriously complicated cases. We report on an adult male with scrub typhus complicated with acute fulminant myocarditis with no previous comorbid illness who recovered successfully with proper treatment including antibiotics, ventilator support, percutaneous cardiopulmonary support, and continuous renal replacement therapy.

Citations

Citations to this article as recorded by  
  • Comprehensive review on cardiac manifestation of scrub typhus
    Barath Prashanth Sivasubramanian, Abul Hasan Shadali Abdul Khader, Diviya Bharathi Ravikumar, Francis Vino Dominic Savio, Umabalan Thirupathy, Varshini Thiruvadi, Rhea Prasad, Hema Thokala, Husna Qadeer, Dhiraj Poragal Venkataperumal, Ashima Gupta, Nagara
    Frontiers in Tropical Diseases.2024;[Epub]     CrossRef
  • Case Report: Fulminant Myocarditis Successfully Treated With Extracorporeal Membrane Oxygenation in Ikeda Strain Orientia tsutsugamushi Infection
    Hyejin Park, Yongwhan Lim, Min Chul Kim, Seong Eun Kim, In-Seok Jeong, Yoo Duk Choi, Dong-Min Kim
    Frontiers in Cardiovascular Medicine.2021;[Epub]     CrossRef
  • A case report of scrub typhus complicated with myocarditis and rhabdomyolysis
    Young-Jae Ki, Dong-Min Kim, Na-Ra Yoon, Sung-Soo Kim, Choon-Mee Kim
    BMC Infectious Diseases.2018;[Epub]     CrossRef
  • 53 View
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  • 3 Crossref
[English]
Hepatic Actinomycosis with Abdominal Wall and Paracolic Gutter Involvement
Tae Hoon Kim, Myung Shin Kang, Dong Hee Shin, Ji Hye Lee, Jungok Kim
Ewha Med J 2016;39(1):6-9.   Published online January 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.1.6

A 53-year-old female with intrauterine contraceptive device insertion was admitted for painful abdominal mass on the left upper quadrant abdomen. Abdominal computed tomography scan showed multiple enhancing masses on the right lobe of liver, left abdominal wall and right paracolic gutter. We performed incisional biopsy on the left abdominal wall lesion. Although microorganisms were not identified, the histopathologic result was consistent with actinomycosis which contained sulfur granules within the chronic granulomatous inflammation. She was treated with penicillin agents for 6 months. We report a case of hepatic actinomycosis with abdominal wall and paracolic gutter involvement.

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[English]
Cutaneous Mucormycosis in a Patient with Diabetes Mellitus
Ji Hwan Park, Seo Hwa Park, Eun Gyu Kang, Gyu Cheon Kyung, Hyo Dong An, So-Yeon An
Ewha Med J 2016;39(1):10-13.   Published online January 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.1.10

Mucormycosis is a rare disease caused by fungi. Most commonly involved sites of mucormycosis infection are sinuses, lungs, skin and soft tissues. Systemic risk factors for mucormycosis are diabetes mellitus, neutropenia, corticosteroid use, hematological malignancies, organ transplantation, metabolic acidosis, deferoxamine use and advanced age. Local risk factors are history of trauma, burns, surgery and motor vehicle accidents. We present a case of cutaneous mucormycosis in a patient with diabetes mellitus. A 66-year-old female with uncontrolled diabetes mellitus, admitted with necrotizing lesion after minor abrasions on leg. We took a culture of the lesion and it is diagnosed with mucormycosis. Disease progressed despite administration of systemic amphotericin B. We performed above-knee amputation and changed antifungal agents into liposomal amphotericin B. A tissue biopsy showed nonseptate, irregularly wide fungal hyphae with frequent right-angle branching. Our case report suggests that patients with risk factors should be observed carefully.

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  • Epidemiology and Treatment Outcome of Mucormycosis in Khuzestan, Southwest of Iran
    Roohangiz Nashibi, Sara Afzalzadeh, Mohammad Javad Mohammadi, Ahmad Reza Yari, Farid Yousefi
    Archives of Clinical Infectious Diseases.2016;[Epub]     CrossRef
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  • 1 Crossref
[English]
Paroxetine-induced Hypoglycemia in Type 2 Diabetic Patient
Seunghee Han, Hye-Sun Park, Yong-ho Lee, Byung-Wan Lee, Eun Seok Kang, Bong-Soo Cha
Ewha Med J 2016;39(1):14-16.   Published online January 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.1.14

Selective serotonin reuptake inhibitors are commonly prescribed drugs for the treatment of depression in the patients with diabetes. Here, we report a case of paroxetineinduced severe recurrent hypoglycemia that developed in a 35-year-old woman with poorly controlled type 2 diabetes complicated by diabetic nephropathy and neuropathy. She discontinued her daily insulin therapy 2 months after the introduction of paroxetine, but hypoglycemic events were sustained. After discontinuation of paroxetine, no more hypoglycemic events occurred.

Citations

Citations to this article as recorded by  
  • Pharmacological treatment for mental health illnesses in adults receiving dialysis: A scoping review
    Jenny Wichart, Peter Yoeun, Tracy Chin, Christopher Evernden, Charlotte Berendonk, Jodi Kerr, Alexandra Birchall, Belinda Boschee, Kimberly Defoe, Jasleen Dhaliwal, Tasia KarisAllen, Megan Kennedy, Alexis McDonald, Monika K. Mierzejewski, Kara Schick‐Maka
    Fundamental & Clinical Pharmacology.2024; 38(5): 862.     CrossRef
  • Paroxetine

    Reactions Weekly.2016; 1597(1): 166.     CrossRef
  • 62 View
  • 4 Download
  • 2 Crossref
[English]
Isolated Myeloid Sarcoma Presenting as Cord Compression by Paraspinal Mass
Hyun Ho Oh, Hyun-Jung Kim, Tae-Hee Han, Min Kwan Kwon, Soo Ya Bae, Young Jin Yuh
Ewha Med J 2016;39(1):17-22.   Published online January 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.1.17

Myeloid sarcoma is a rare tumor mass consisting of immature granulocytic cells occurring in an extramedullary site or in a bone. It has often been observed during the course of an acute leukemia, myelodysplastic syndrome or myeloproliferative neoplasms, and it can involve any site of the body. However, it rarely present in the absence of bone marrow infiltration, especially for the isolated spinal myeloid sarcoma. In this report, we describe a case of isolated myeloid sarcoma that showed spinal compression. A 66-year-old male, with no underlying disease or medication history, presented with a progressive back pain and numbness in bilateral lower extremities that had begun two weeks before. He was diagnosed with myeloid sarcoma with no evidence of bone marrow involvement. Tumor cells were positive for CD34, c-KIT, and Bcl-2 on the immunohistochemical stain. He was treated with systemic chemotherapy with daunorubicin plus cytosine arabinoside and achieved a partial response.

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[English]
Tocilizumab-induced Transaminitis in a Seropositive Rheumatoid Arthritis Patient with Macrophage Activation Syndrome
Byung-woo Yoo, Cheol Keun Park, Hae Ryong Yun, Daehoon Kim, Soo-Kon Lee, Sang-Won Lee
Ewha Med J 2016;39(1):23-27.   Published online January 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.1.23

As a new humanized monoclonal antibody against the interleukin-6 receptor, tocilizumab is currently used for the treatment of rheumatoid arthritis (RA) patients. Tocilizumab was reported to provoke drug-related liver toxicity, although there have been no reports on significant liver toxicity from tocilizumab in Korean patients with RA to date. Here, we describe the first case of tocilizumab-related liver toxicity in a patient with complicated RA, accompanied with macrophage activation syndrome, who had received tacrolimus and prednisolone and in whom both conventional disease modifying anti-rheumatic drugs, including methotrexate, leflunomide and sulfasalazine or tumor necrotizing factor-α blockades, were contraindicated due to drug eruption and a history of lung cancer.

Citations

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  • Tocilizumab

    Reactions Weekly.2016; 1597(1): 198.     CrossRef
  • 46 View
  • 0 Download
  • 1 Crossref
[English]
Solitary Rectal Ulcer Syndrome Mimicking Rectal Cancer
Young Min Choi, Hyun Joo Song, Min Jung Kim, Weon Young Chang, Bong Soo Kim, Chang Lim Hyun
Ewha Med J 2016;39(1):28-31.   Published online January 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.1.28

Solitary rectal ulcer syndrome (SRUS) is a rare benign and chronic rectal disease that has a wide spectrum of clinical presentations and variable endoscopic findings. It is usually diagnosed by histopathological examination through biopsy. A 68-year-old man was referred to our hospital with anal pain and difficulty on bowel movement. Colonoscopy showed a hemorrhagic ulcerated mass in the rectum. All radiologic findings such as abdominopelvic computed tomography (CT), positron emission tomography-CT and magnetic resonance imaging were suspicious of rectal cancer. Although the patient underwent repeat endoscopic biopsy and one surgical biopsy, the results were not indicative of malignancy. Two months after conservative management, clinical symptoms and colonoscopic findings were markedly improved. Thus, we report this rare case of a 68-year-old man who had a central ulcerated mass that mimicked rectal cancer on gross colonoscopic and radiologic findings, representing an SRUS variant.

Citations

Citations to this article as recorded by  
  • Ultrasonography of solitary rectal ulcer syndrome (review and case reports)
    A. E. Pershina, Yu. L. Trubacheva, D. V. Vyshegorodtsev, O. M. Biryukov
    Koloproktologia.2022; 21(4): 100.     CrossRef
  • Solitary rectal ulcer syndrome
    Mojgan Forootan, Mohammad Darvishi
    Medicine.2018; 97(18): e0565.     CrossRef
  • A Case of Solitary Rectal Ulcer Syndrome in a 16-year-old Girl Presented with Iron Deficiency Anemia
    Sun Hee Jung, Young Bae Kim, Hyun Jin Kim, Jin Won Hwang, Sang Heon Lee, Su Jin Jung, Ji Kyoung Park
    Clinical Pediatric Hematology-Oncology.2016; 23(1): 53.     CrossRef
  • 53 View
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  • 3 Crossref
[English]

Prostatic abscess is not a common entity which is characterized by non-specific clinical presentations. This poses a diagnostic challenge for clinicians. Clinicians routinely consider antibiotic treatments concomitantly with drainage for the treatment of prostatic abscess. But there are no established guidelines for its optimal timing, methods and indications. Surgical drainage procedures include transurethral resection of the prostate and perineal incision and drainage. But there is variability in the prognosis of patients between the procedures. We have treated a 48-year-old diabetes patient with prostatic abscess accompanied by MRSA bacteremia using a percutaneous fine-needle aspiration under the computed tomography (CT) guidance. The patient achieved improvement of the symptoms and in follow up CT findings. A percutaneous drainage under the CT guidance is advantageous in that it causes fewer complications. However, Further studies are warranted to establish the optimal timing, methods and indications in patients with prostate abscess.

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