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Volume 39(3); July 2016

Original Article

[English]
Anemia in Individuals over Age 80: Unattended Issue in Clinical Practice
Yun Jin Jeong, Joo Kyoung Cha, Hyun Jung Lee, Seok Lae Chae, Hee Jin Huh, Jae-Woo Chung, Do Yeun Kim
Ewha Med J 2016;39(3):69-75.   Published online July 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.3.69
Objectives

To assess the current state of anemia evaluation in the elderly over 80 years of age.

Methods

Patients who were more than 80 years old and visited Dongguk University Ilsan Hospital from April 2005 to February 2014 were included. Statistical analysis were assessed using the logistic regression model.

Results

Total 548 patients, who had anemia according to WHO criteria, were identified. The median age was 85 years old (range, 82 to 99 years) and median hemoglobin level was 11.0 g/dL (range, 2.7 to 12.9 g/dL). Twenty-eight, 468, and 52 patients were classified as microcytic anemia, normocytic anemia, and macrocytic anemia, respectively. Among them, 397 patients (72.4%) did not undergo proper evaluation for the cause anemia i.e., 8 cases (28.5%) of microcytic anemia, 361 cases (77.1%) of normocytic anemia, and the 28 cases (53.84%) of 52 macrocytic anemia patients. The remaining 151 patients (27.6%) had completed the evaluation, and 24 patients (15.9%) were diagnosed as solid malignancies. In the assessment of iron deficiency anemia, hemoglobin levels, and age had no effect on whether or not to perform esophagogastroduodenoscopy.

Conclusion

This finding showed that physicians often neglected anemia in individuals over 80 years of age. Though these patients have limited life expectancy, physicians should carefully discriminate the sub-population who will be benefit from adequate evaluation and treatment.

Citations

Citations to this article as recorded by  
  • High anemia prevalence in Korean older adults, an advent healthcare problem: 2007–2016 KNHANES
    Hee Won Chueh, Hye Lim Jung, Ye Jee Shim, Hyoung Soo Choi, Jin Yeong Han
    BMC Geriatrics.2020;[Epub]     CrossRef
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  • 1 Crossref

Case Reports

[English]
Living Donor Liver Transplantation in a Hepatitis B Patient with Acute on Chronic Liver Failure Accompanying Hepatocellular Carcinoma
Hee Jin Hong, Joo Ho Lee, Yun Bin Lee, Hana Park, Seong Gyu Hwang, Kyu Sung Rim
Ewha Med J 2016;39(3):76-80.   Published online July 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.3.76

Acute clinical deterioration in patients with chronic liver disease is called acute on chronic liver failure (ACLF). Principles of management of ACLF consist of early identifying etiology of liver disease, rapid intervention of precipitating event and discreet intensive cares. Despite medical intensive cares, if liver failure progresses, liver transplantation could be the other option. Also, liver transplantation is the only treatment that offers a chance of cure for hepatocellular carcinoma (HCC) and the underlying liver cirrhosis simultaneously. Emergent living donor liver transplantation (LDLT) can be performed for patients with acute liver failure and improves survival rate, especially in circumstances which liver graft is often not available because of deceased donors are not affordable. Here, we describe a chronic hepatitis B patient who developed ACLF accompanying early HCC. Because he did not improved with medical care, he received emergent LDLT. After LDLT, he showed great improvement without critical complications.

Citations

Citations to this article as recorded by  
  • Systematic review with meta‐analysis: liver transplant provides survival benefit in patients with acute on chronic liver failure
    Mohamed A. Abdallah, Muhammad Waleed, Matthew G. Bell, Morgan Nelson, Robert Wong, Vinay Sundaram, Ashwani K. Singal
    Alimentary Pharmacology & Therapeutics.2020; 52(2): 222.     CrossRef
  • 65 View
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  • 1 Crossref
[English]
Herpes Simplex Virus Hepatitis Treated with Acyclovir
Beom Jin Jeong, Hye Jin Tae, Young Jun Cho, Yeong Mo Kang, Eun Lee, Sang Jo Han, Jeong Mi Shin
Ewha Med J 2016;39(3):81-84.   Published online July 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.3.81

Herpes simplex viruses (HSVs) are the most common cause of mucocutaneous infections with dissemination to visceral organs. HSV-induced hepatitis is a rare but frequent cause of hepatitis in immunocompromised patients, pregnant women, and newborns. However, diagnosis is often difficult because the clinical features are nonspecific. In addition, the HSV-related mortality rate is high. Signs and symptoms of HSV include fever, anorexia, nausea, vomiting, abdominal pain or tenderness, leukocytopenia, coagulopathy, and an increase in serum transaminase levels without jaundice. We present a patient who did not correspond to the above symptoms, but survived following prompt intravenous high-dose acyclovir provided early in the course of the disease.

Citations

Citations to this article as recorded by  
  • A Surprising Cause of Liver Abscesses in a Post-Chemotherapy Patient: Herpes Simplex Virus
    Rukevwe Ehwarieme , Apeksha N Agarwal, Rahaf Alkhateb , Jason E Bowling, Gregory M Anstead
    Cureus.2021;[Epub]     CrossRef
  • Herpes hepatitis as a complication of total abdominal hysterectomy; an unusual complication of abdominal instrumentation
    Muharrem Yunce, Pavan Bhat, Daisy Jaganathan, Michelle Bahrain
    Clinical Case Reports.2019; 7(1): 11.     CrossRef
  • A Rare Case of Herpes Simplex Virus-2 Hepatitis with Negative Serology
    Mohanad Soliman, Olalekan Akanbi, Ihab Almagdub, Kishore Karri, Pradeep Yarra, Saad Emhmed Ali, Hanine El Haddad
    Case Reports in Hepatology.2019; 2019: 1.     CrossRef
  • 72 View
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  • 3 Crossref
[English]
Progressive Pituitary Involvement in a Patient with Localized Granulomatosis with Polyangiitis
Hyeonkyeong Jeon, In Je Kim, Young Sun Hong, Soo Mee Lim, Min Sun Cho, Jisoo Lee
Ewha Med J 2016;39(3):85-88.   Published online July 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.3.85

Localized granulomatosis with polyangiitis (loc-GPA) is a milder disease state of GPA restricted to the respiratory tract. Transition from localized form to systemic/generalized disease is predicted to occur in approximately 10% of the patients. We report an unusual case of loc-GPA involving multiple cranial nerves, which in 3 years progressed into systemic disease involving pituitary gland. Initially antineutrophil cytoplasmic antibody (ANCA) was negative, but as symptoms of diabetes insipidus started, ANCA became positive. Clinical course of ANCA negative loc-GPA should be carefully monitored for development of systemic disease. ANCA may be a useful marker for detecting transition from localized to systemic disease.

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[English]
Durable Response to Pazopanib in a Patient with Metastatic Alveolar Soft Part Sarcoma
Jimin Han, Im Il Na, Min Woo Jung, Su Heui Lee, Jae Woon An, Jae Soo Koh
Ewha Med J 2016;39(3):89-92.   Published online July 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.3.89

Alveolar soft part sarcoma (ASPS) is a rare form of soft tissue sarcoma, and frequently, metastases are found at diagnosis. In patients with metastatic or unresected ASPS, systemic treatment is extremely limited, because conventional chemotherapeutic agents have not been effective in most cases. A novel agent inhibiting angiogenesis, pazopanib, has been proven to be effective for metastatic soft tissue sarcoma in a second-line setting. However, the efficacy of pazopanib in ASPS has not yet been reported. A 22-year-old man presented with right calf ASPS and multiple lung metastases. Pazopanib as a second-line treatment showed significant tumor response. To the best of our knowledge, this is the first report of the effectiveness of pazopanib in ASPS.

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Images and Solutions
[English]
Magnetic Resonance Imaging of Dermatomyositis with Bilateral Involvement of the Erector Spinae Muscle
Shinjiro Kaieda, Masaki Okamoto, Shiroh Miura, Hiroaki Ida
Ewha Med J 2016;39(3):93-94.   Published online July 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.3.93
  • 26 View
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[English]
Primary Pulmonary Hodgkin Lymphoma Associated with Primary Sjögren's Syndrome
Masashi Ohe, Satoshi Hashino, Katsura Nagai, Atsuo Hattori, Ken Furuya
Ewha Med J 2016;39(3):95-98.   Published online July 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.3.95
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