• Title/Summary/Keyword: Old Literatures

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A Case of Cystic Degeneration of Uterine Adenomyosis (낭성 변화를 일으킨 자궁선근증 1례)

  • Kwak, Yang-Soo;Lee, Sang-Won;WhangBo, Ho-Joon;Lee, Doo-Jin;Lee, Sung-Ho
    • Journal of Yeungnam Medical Science
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    • v.11 no.2
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    • pp.405-410
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    • 1994
  • Adenomyosis is a common disease of middle-aged women and adenomyoma is a variety of adenomyosis that formed localized tumor. Cystic degeneration of an adenomyoma is a rare clinical manifestation. A 30-year-old parous woman suffered from severe dysmenorrhea and menorrhagia for about 5 months, was operated under the impression of endometriosis of the pelvis. Following the operation, cystic degeneration of an adenomyoma was found incidentally. The authors experienced a case of adenomyosis that formed cystic tumor of uterus and presented with a pertinent literatures.

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Knee Arthroscopy in the Obese: A Case Report (비만환자에서 시행한 슬관절 관절경술 - 증례 보고 -)

  • Baek, Seung-Hoon;Kim, Shin-Keun
    • Journal of the Korean Arthroscopy Society
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    • v.14 no.1
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    • pp.29-32
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    • 2010
  • Several reports have described the increased perioperative risks as well as surgical techniques for performing various procedures in obese patients. However, few reports have addressed the effects of obesity on routine arthroscopic procedures known to be common and safe. Describing the case of a partial meniscectomy performed in a 17-year-old male with a body weight of 120 kg, we review literatures published to the present and provide technical problems and possible complications that can occur when performing routine knee arthroscopy in bariatric patients.

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Rhinocerebral Mucormycosis with Intracerebral Hemorrhage (뇌실질내 출혈을 동반한 비뇌 모균증)

  • Shin, Pill Jae;Lee, Ho Kook;Kim, Chang Hyun;Yang, Kyung Hun;Hwang, Do Yun
    • Journal of Korean Neurosurgical Society
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    • v.29 no.1
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    • pp.136-142
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    • 2000
  • Rhinocerebral mucormycosis is a rare but acutely fatal disease caused by fungi belonging to the order Mucorales, and characterized by an aggressive necrotizing infection spreading from the nose to the paranasal sinuses, orbit, and then to the central nervous system. It most frequently develops in individuals with poorly controlled diabetes mellitus. The authors report a 65-year-old woman who developed intracerebral hemorrhage during treatment for rhinocerebral mucormycosis associated with diabetes mellitus. Despite the treatment, she became worse. The pertinent literatures were reviewed.

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Primary Intracranial Leptomeningeal Melanomatosis

  • Kim, Do-Hyoung;Choi, Chan-Young;Lee, Chae-Heuck;Joo, Mee
    • Journal of Korean Neurosurgical Society
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    • v.58 no.6
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    • pp.554-556
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    • 2015
  • Primary intracranial malignant melanoma is a very rare and highly aggressive tumor with poor prognosis. A 66-year-old female patient presented a headache that had been slowly progressing for several months. A large benign pigmented skin lesion was found on her back. A brain MRI showed multiple linear signal changes with branching pattern and strong enhancement in the temporal lobe. The cytological and immunohiostochemical cerebrospinal fluid examination confirmed malignant melanoma. A biopsy confirmed that the pigmented skin lesion on the back and the conjunctiva were benign nevi. We report a case of primary intracranial malignant melanoma and review relevant literatures.

Strategy for the Patient with Tuberculum Sellae Meningioma Combining Bilateral Internal Artery Aneurysm

  • Cha, Ki-Yong;Park, Sang-Keun;Hwang, Yong-Soon;Kim, Tae-Hong
    • Journal of Korean Neurosurgical Society
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    • v.38 no.2
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    • pp.151-154
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    • 2005
  • A 43-year-old woman was admitted with the chief complaint of progressive visual disturbance and her brain radiological studies disclosed well demarcated tumor at tuberculum sellae area and bilateral mirror image paraclinoid internal carotid artery saccular aneurysms. A larger left side aneurysm was pointing medialy and almost encased by the tumor. Although a brain tumor and intracranial aneurysm can be simultaneously treated by surgery, the high risk of intra-operative aneurysm rupture should be considered. Therefore, the author secondly performed tumor resection after the endovascular embolization of the aneurysm which was embedding the tumor using a Guglielmi detachable coil. After successful treatment of the patient with tuberculum sellae meningioma associated with bilateral mirror image paraclinoid aneurysms using endovascular and surgical techniques, the authors present the case with a review of the related literatures.

Histopathologic Classification of Salivary Gland Neoplasm (경부기관에 발생한 선양낭성암종 1예)

  • 추호석;정은재;권순영;정광윤
    • Korean Journal of Bronchoesophagology
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    • v.9 no.1
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    • pp.75-78
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    • 2003
  • Primary adenoid cystic carcioma of trachea is rare, with an incidence of only 0.2 per 100,000 persons per year. When all series of the tracheal carcinomas are combined, adenoid cystic carcinoma is the second most common tumor only to squamous cell carcinoma in incidence. Most patients have wheezing or stridor, dyspnea, hemoptysis, and cough as symptoms. Treatment options include surgery alone, radiation therapy alone, or a combination of both. The recommended surgical option is primary tracheal resection and reconstruction. Recently, we experienced a case of adenoid cystic carcinoma in 45 year old female patient who was treated tracheal tumor resection and end-to-end anastomosis of the trachea, so we report this case with the literatures.

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Surgical Management of Occult Foreign Body in the Bronchus Intermedius (중간 기관지 내 이물의 수술적 치료)

  • Kim, Jae-Bum;Park, Chang-Kwon
    • Korean Journal of Bronchoesophagology
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    • v.16 no.1
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    • pp.51-54
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    • 2010
  • Occult bronchial foreign body is that long-standing foreign body lodge in bronchial tree. Occult bronchial foreign bodies arc rare in adults, whereas tracheobronchial aspiration of foreign bodies occurs commonly in children. A 65-year-old man with chronic cough, sputum production, and fever was transferred for treatment of right middle and lower lobc collapse and obstructive pneumonitis as evidenced by imaging studies. The patient was treated with right middle-lower bilobectomy because fiberoptic bronchoscopic removal of the foreign body failed. We report this case with review of literatures.

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A Case of Multiple Endobronchial Hamartomas (다발성 기관지내 과오종 1예)

  • Park, Sung-Kyu;Rhee, Kyoung-Joo;Park, Mee-Ja;Kim, Sun-Young
    • Tuberculosis and Respiratory Diseases
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    • v.39 no.1
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    • pp.83-88
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    • 1992
  • A hamartoma can be defined as a developmental malformation composed of tissue that normally constitute the organ in which the tumor occurs, but in which the tissue elements, although mature, are disorganized. Hamartoma is one of the most common benign lung tumors. Most of them are located in the lung parenchyme, but very rarely it can originate endobronchially. There is no case report of multiple endobronchial hamartomas in Korea. We report a case of multiple endobronchial hamartomas in a 63 year old woman with a review of the literatures.

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The Calcifying Epithelial Odontogenic Tumor: Report of a Case (석회화 상피성 치성종양의 증례보고)

  • Lee Seung-Hyun;Hwang Eui-Hwan;Lee Sang-Rae;Hosaka Mitsuo
    • Journal of Korean Academy of Oral and Maxillofacial Radiology
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    • v.28 no.2
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    • pp.521-537
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    • 1998
  • The calcifying epithelial odontogenic tumor is a rare benign odontogenic neoplasm which was first described by Pindborg in 1955 and accounts for less than 1% of all odontogenic tumors. The tumor occurs primarily in the molar-premolar region of the mandible, and 52% of cases are associated with an unerupted tooth. The clinical feature is most commonly a slow-growing painless swelling. The tumor may show considerable radiographic variation and usually characteristic histopathologic features. In this study, we report a case of the calcifying epithelial odontogenic tumor on the left mandibular body and ramus area in a 28-year-old male with a brief review of the concerned literatures.

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A Case of Lymphangioleiomyomatosis Looked Like Miliary Tuberculosis (속립성 결핵으로 오인된 폐임파관평활근종증)

  • Won, Kyoung-Sook;Park, Keun-Uk;Park, Hyun-Jin;Kim, In-Soo;Jeong, Yeon-Tae
    • Tuberculosis and Respiratory Diseases
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    • v.42 no.2
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    • pp.244-249
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    • 1995
  • We experienced one case of pulmonary lymphangioleiomyomatosis in 26-year-old female patient. She had taken antituberculous medication under the impression of miliary tuberculosis on simple chest X-ray at peripartum period. On outpatient follow-up she complained of progressive exertional dyspnea in spite of medication. Through careful history taking and physical examination, high resolutional CT, and open lung biopsy she was diagnosed as pulmonary lymphangioleiomyomatosis combined with incomplete type of tuberous sclerosis. So, we presented the case with the brief review the literatures.

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