• Title/Summary/Keyword: Rarity

Search Result 318, Processing Time 0.027 seconds

Extraskeletal Osteogenic Sarcoma of the Mediastinum; 1 Case Report (종격동에 발생한 골외성 골육종;1례 보고)

  • Won, Tae-Hui;Kim, Ju-Hyeon
    • Journal of Chest Surgery
    • /
    • v.26 no.5
    • /
    • pp.413-416
    • /
    • 1993
  • Extraskeletal osteogenic sarcoma is a rare malignant tumor of soft tissue, and its predilection sites are the extremity, retroperitoneum, trunk, and the head and neck area. To our knowledge 5 cases of primary involvement of the mediastinum have been reported. Because of its rarity and difficulty in exact diagnosis preoperatively, we report an extraskeletal osteogenic sarcoma in the anterior mediastinum. The patient was a thirty eight old male. He complained of cough and sputum over 2 months. The chest roentgenogram and the chest MRI[magnetic resonance image] were done and showed anterior mediastinal mass with calcification. Excision of the mass was done under the preoperative impression of thymoma, and the pathologic report was extraskeletal osteogenic sarcoma of the mediastinum.

  • PDF

A case of diaphragmatic hernia associated with pregnancy (임신으로 인한 횡격막 탈장 1례)

  • Sohn, Kwang-Hyun;Lee, Nam-Soo;Lee, Geon-ju
    • Journal of Chest Surgery
    • /
    • v.13 no.2
    • /
    • pp.154-157
    • /
    • 1980
  • A twenty three year old, Primigravida and 32 week pregnant woman who has been complained dyspnea, chest pain, nausea and vomiting was admitted to this chest surgical department on Feb. 19, 1979. Physical findings were those of acutely ill appearance, decreased thoracic excursion and absence of breath sounds in the left hemithorax. Roentgen examination of the chest revealed reticular cystic densities in the left, particularly in lower lung field with collapse of the left lung. Correction of the diaphragmatic hernia was carried out with reduction and repair of the hernia through transperitoneal approach. On exploration, the defect of the diaphragm was 12 x 12 cm in size and was located posterolateral area of left diaphragm. Hernia contents were stomach, spleen, omentum and splenic flexure of large bowel. The baby was normal full term spontaneous delivered at 36th POD. Diaphragmatic hernia complicated by pregnancy is a rarity and mortality is extremely high. Therefore, the literatures have reviewed and the case is reported.

  • PDF

Glomus Tumor in Left Main Bronchus (좌측 주기관지에 위치한 사구종양)

  • 곽기오;김병훈;이양행;조광현
    • Journal of Chest Surgery
    • /
    • v.32 no.8
    • /
    • pp.761-764
    • /
    • 1999
  • The glomus tumor is a distinctive benign neoplasm with a small painful nodule, occurs most commonly in extremities but may be found elsewhere in the body. Its occurrence in the trachea or lung parenchyme has been recognized with extreme rarity and there has not been any report, to our knowledge, of its occurrence in the main bronchial glomus tumor. We report a case of a glomus tumor in the left main bronchus in a 67-year-old man who was presented with blood-tinged sputum and dyspnea, which was completely relieved by surgical resection.

  • PDF

Development of Forest Ecosystem Evaluation Considering Biotope Type (비오톱 유형을 고려한 산림지역 생태계 평가기법 개발)

  • Kim, Jeong Ho
    • Journal of the Korean Society of Environmental Restoration Technology
    • /
    • v.10 no.3
    • /
    • pp.38-51
    • /
    • 2007
  • The purpose of this study is to analyze of biotope types and to develop assessment for forest ecosystem evaluation method. Vegetation types divided into 27 types. Considering the vegetation types, vegetation structures, DBH, potentials, and disturbance, it was decided to apply 58 biotope types and survey site's biotopes were divided into 24 biotope types. Assessment indicators were naturaliness, diversity, rarity, stability, potential, and disturbance. The areas given the first grade in ecological value included 9.2% of the site's total land. Areas with the second grade accounted for 43.0% of the total land. Areas with the third grade made up 47.8% of the site and mostly they were areas with dominance of fired area and artificial forest. To plan to build naturally-development for Site, there should be plans to conserve areas with the first grades. For the areas with the second, and third grades, plans for ecological land use based on conservation and restoration in terms of securing biodiversity are needed.

A Case of Myelopathy after Intrathecal Injection of Fluorescein

  • Park, Kwang-Yeol;Kim, Young-Baeg
    • Journal of Korean Neurosurgical Society
    • /
    • v.42 no.6
    • /
    • pp.492-494
    • /
    • 2007
  • We present a case with seizure, confusion, hypesthesia and paraplegia after intrathecal injection of fluorescein. A 41-year-old man was admitted to our institution for the management of the CSF leakage. Intrathecal injection of fluorescein was performed and he complained of severe pain and numbness in the lower extremities at the end of the injection. Four hours later, he exhibited confusion, paraparesis and two episodes of generalized seizures. Two days later, he showed paraplegia and all sensory modalities below the T12 level were absent. Spine magnetic resonance imaging revealed myelopathic change in the lower thoracic spinal cord. There was no improvement of weakness and sensory deficits in lower extremity even 14 days after fluorescein injection. We speculated that thoracic myelopathy was associated with the intrathecal injection of fluorescein. In spite of its rarity, the complication after intrathecal injection of fluorescein could be serious. Thus, obtaining an informed consent with discussion with patient before the procedure is mandatory.

Intraventricular Cavernous Hemangiomas Located at the Foramen of Monro

  • Lee, Byung-Jou;Choi, Chan-Young;Lee, Chae-Heuck
    • Journal of Korean Neurosurgical Society
    • /
    • v.52 no.2
    • /
    • pp.144-147
    • /
    • 2012
  • Intraventricular cavernous hemangiomas are uncommon. Among them, those occurred at the foramen of Monro in the third ventricle may be of particular interest because of its rarity, development of hydrocephalus, being differentiated from other brain lesions. We present a rare case of intraventricular cavernous hemangioma at foramen of Monro which was resected through microsurgery and also review the relevant literatures.

Diagnosis of Persistent Primitive Olfactory Artery Using Computed Tomography Angiography

  • Kim, Myoung-Soo;Lee, Ghi-Jai
    • Journal of Korean Neurosurgical Society
    • /
    • v.49 no.5
    • /
    • pp.290-291
    • /
    • 2011
  • Persistent primitive olfactory artery (PPOA) is a rare anomaly of the anterior cerebral artery. We present one case of PPOA incidentally diagnosed with the aid of computed tomography (CT) angiography. A 24-year-old woman was admitted to our hospital after sudden onset of vertigo. Three-dimensional CT angiography revealed an anomalous artery arising from the terminal portion of the right internal carotid artery. The proximal portion of the anomalous artery coursed anteromedially and made a hairpin turn posterosuperior to the midline. PPOA may be overlooked because of its rarity, but CT angiography can be useful in detecting this rare vascular anomaly. Follow-up study is necessary in our case to confirm whether an aneurysm occurs on the PPOA.

Chordoid Glioma : A Case Report of Unusual Location and Neuroradiological Characteristics

  • Kim, Jin-Wook;Kim, Jae-Hyoung;Choe, Ghee-Young;Kim, Chae-Yong
    • Journal of Korean Neurosurgical Society
    • /
    • v.48 no.1
    • /
    • pp.62-65
    • /
    • 2010
  • Since the World Health Organization (WHO) classification for central nervous system neoplasms was declared in 2000, chordoid glioma of the third ventricle has been noted as a newly recognized tumor for central nervous system neoplasms. Although there is not enough universal experience to know the nature of this tumor due to its rarity, the origin of chordoid glioma was guardedly proposed to be the ependymal cells of the third ventricle. Such an idea has been primarily based on the specific location of the tumor, that is, third ventricle, suprasellae, and hypothalamus. However, we report a rare case of histologically confirmed chordoid glioma located in the left thalamus, not attached to any of the midline structures having unusual neuroradiological characteristics.

Various craniofacial clefts (다양한 두개안면 파열)

  • Baek Seung-Hak;Lee Jin-Kyung;Kim Na-Young;Kim Tae-Kyung
    • Korean Journal of Cleft Lip And Palate
    • /
    • v.6 no.2
    • /
    • pp.117-130
    • /
    • 2003
  • The prevalence of craniofacial cleft is reported to be 10-34 / 100,000 live birth of human. This case report describes the characteristics of the Tessier classification number 0, 5, 7, and 14 craniofacial cleft patients. Given the rarity and unique nature of the clinical expression of each of the craniofacial clefts, the treatment plans can not be standardized but must be based on the individual assessment of each case.

  • PDF

Treatment of Ednometrial Carcinoma Stage II

  • Han I.;Kanellitsas C.;Kumar N.;Amendola B.;Morley G.
    • Radiation Oncology Journal
    • /
    • v.2 no.2
    • /
    • pp.253-260
    • /
    • 1984
  • Between January 1971 and December 1580 fifteen patients diagnosed of adenocarcinoma of the endometrium, stage II seen and treated at the University of Michigan Hospitals. are reviewed. Ten patients were treated with radiation therapy alone. five received hysterectomy after radiation. The five year survival of the patients receiving radiation and surgery was $100\%$ although one of them died after 62 month aster treatment. Of those receiving radiotherapy alone two died at i and 24months after therapy. All of the patients died of distant metastasis. Radiation cystitis was observed among surgically treated patients. while proctitis was observed in 3 cases receiving radiation alone. Though the number of cases reported is small due to rarity of the disease. it appears that radiation alone could provide reasonable tumor control. Also it appears that preoperative irradiation might lead to a longer survival. One patient who survived 62 months had para-aortic node involvement.

  • PDF