• Journal of Chest Surgery
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• 제12권4호
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• pp.379-382
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• 1979

Cavernous lymphangioma is a benign tumor of lymphatic origin encountering most frequently in young children, and composed of softly fluctuated monolocular or multilocular cystic masses which developed from embryonic outpouching of the venous system. The prevailing site of this tumor Is at the anterolateral neck region particularly posterior triangle, and occasionally axillary, mesentery and spleen etc. Recently, we have experienced one case of left axillary cavernous lymphangioma, which surgically removed successfully and confirmed histopathologically. We want to report one case of left axillary large cavernous lymphangioma with a brief review of the relevant literatures.

• Journal of Chest Surgery
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• 제31권3호
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• pp.324-328
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• 1998

식도에 발생하는 혈관종은 식도에 드물게 발생하는 양성종양의 2% 내지 3% 정도 차지할 정도로 매우 희귀하여 세계적으로 보고된 증례수가 많지 않다. 저자들은 식도에 발생한 매우 희귀한 해면혈관종 1례를 수술치험하였기에 문헌고찰과 더불어 보고하고자 한다. 환자는 40세 남 米\ulcorner경미한 연하장애를 주소로 내원하여 식도조영술, 식도 내시경검사, 조영제를 이용한 흉부 전산화 단층촬영등을 시행하여 하부 식도의 점막하층에서 발생하여 근육층 밖으로 돌출되어 나온 식도 종양이 추정되어 수술을 시행하였다. 수술소견상 하부 식도 및 식도-위 문합부에 걸쳐 과혈관성의 7x7x3.5cm 크기의 거대한 종괴가 식도점막하층과 식도근육층 그리고 주위조직으로의 침범이 심하게 되어 있어 종양을 포함한 식도절제술 및 식도-위 문합술을 시행하여 병리 조직학적으로 해면 혈관종으로 확진되었으며 환자는 특별한 문제없이 술후 제14일째 건강한 상태로 퇴원하였다.

• 대한정형외과 초음파학회지
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• 제4권2호
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• pp.93-96
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• 2011

저자들은 견갑골의 하내측연과 승모근의 외측연 사이에서 발생한 혈관종으로, 견갑골 밑으로 자라난 부위가 음향 그림자(acoustic shadowing)로 인해 초음파 검사상 확인할 수 없었으나 수술 시 견갑골 밑으로 연결된 긴 자루(peduncle)를 포함한 혈관종이 발견되어 수술적으로 완전 절제후 초음파 검사로 추시하여 관찰한 증례를 보고하고자 한다.

• 대한족부족관절학회지
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• 제14권1호
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• pp.97-100
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• 2010

Hemangioma are not rare tumors. They can be found in almost any of the vascular structures of the body. Hemangiomas involving the deep structures of the extremities may produce extremely difficult therapeutic problems for the orthopedic surgeon. Pigmented villonodular synovitis (PVNS) is a rare proliferative disorder that affects synovium, tendon sheath and bursa. Although the condition can present in any joint, knee joint is the most commonly affected site and only 2.5% of cases occur in foot and ankle joint. We have experienced a patient who has of foot and report an optimal method of surgical treatment. Authors report the result of hemangioma in mid-foot which arise from removal of a pigmented villonodular synovitis that has low out break rate of benign tumor in mid-foot with literature review.

• Journal of Korean Neurosurgical Society
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• 제52권4호
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• pp.407-409
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• 2012

A spinal epidural hemangioma is rare. In this case, a 51 year-old female patient had low back pain and right thigh numbness. She was initially misdiagnosed as having a ruptured disc with possible sequestration of granulation tissue formation due to the limited number of spinal epidural hemangiomas and little-known radiological findings. Because there are no effective diagnostic tools to verify the hemangioma, more effort should be put into preoperative imaging tests to avoid misdiagnosis and poor decisions).

• Journal of Korean Neurosurgical Society
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• 제37권3호
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• pp.173-178
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• 2005

Objective: The goal of this study is to provide the clinical data of patients with brainstem cavernous hemangiomas after treatment with microsurgery or radiosurgery after conducting a retrospective analysis of 21 patients at one institution. Methods: Twenty one patients with brainstem cavernous hemangiomas were treated at the authors' institution between 1995 and 2004 and clinical analysis was performed by retrospective review of medical records and neuroimaging examinations. Thirteen patients underwent microsurgical resection and radiosurgery was performed as an initial treatment in 9 patients. Results: Radical excision was achieved in 12 among 13 patients and transitory neurological deterioration or new neurological deficit developed during the immediate postoperative period in 7 (54%). The final outcomes at 5 - 70 months after surgery were improved in 11 patients (85%) and worsened in 2 patients (15%) compared with the preoperative state. Radiosurgery was performed in 9 patients. During the follow up period from 5 to 70 months there was neurological improvement in 3 patients, no significant change in 3 and deterioration in 3 patients. Two patients developed rebleeding at 5 months, 60 months respectively after radiosurgery. Conclusion: Microsurgery for symptomatic cavernous hemangioma of brainstem can be performed with acceptable morbidity. Fatal complication is rare with careful selection of the optimal operative approach in well selected patients. Radiosurgery is an effective alternative for the lesions which are not accessible by surgical approach, however, there is still a possibility of rebleeding over a long period after radiosurgical treatment and microsurgery should be considered as a treatment with priority for the majority of cases.

• 대한후두음성언어의학회지
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• 제26권1호
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• pp.54-57
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• 2015

Hemangioma is one of the most common benign neoplasm, which occurs about 50% in head and neck region, but laryngeal hemangioma is relatively rare. Hemangioma occurred in larynx can be treated by surgical removal, cryosurgery, and steroid injection. Transoral CO2 laser micorsurgery has been known as useful method for the treatment of laryngeal hemangioma. We have experienced a 54-years old male patient of hemangioma originated in arytenoid area. This mass was removed via transoral approach with 'en bloc' resection by CO2 laser. We report this case regarding the treatment and prognosis of laryngeal hemangioma with review of literatures.

• Journal of Yeungnam Medical Science
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• 제1권1호
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• pp.161-169
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• 1984

저자 등은 상복부종양을 주소로 영남대학병원 내과에 입원하여 거대 간혈관증으로 진단하여 성공적으로 절제해 낸 1례(例)를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

• 대한영상의학회지
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• 제79권6호
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• pp.311-314
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• 2018

유방의 해면상 혈관종은 매우 드문 양성 혈관 종양이다. 임상증상은 보통 만져지지 않는 종괴로, 영상검사에서 우연히 발견되는 경우가 많다. 유방 혈관종은 대개 초음파에서 표재성에 위치한 타원형의 경계가 분명한 종괴로 보이나, 그 외의 다양한 형태로도 보일 수 있어, 수술 전에 이를 영상 검사만으로 진단하는 것은 쉽지 않다. 이에 저자는 만져지는 유방 종괴를 호소하는 68세 여자에서, 추적 초음파 검사에서 그 크기가 증가한 해면상 혈관종 증례를 보고하고자 한다.

• Journal of Korean Neurosurgical Society
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• 제43권4호
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• pp.198-200
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• 2008

Giant cavernous malformations (GCMs) occur very rarely and little has been reported about their clinical characteristics. The authors present a case of a 20-year-old woman with a GCM. She was referred due to two episodes of generalized seizure. Computed tomography and magnetic resonance image demonstrated a heterogeneous multi-cystic lesion of $7\times5\times5$ cm size in the left frontal lobe and basal ganglia, and enhancing vascular structure abutting medial portion of the mass. These fingings suggested a diagnosis of GCM accompanying venous angioma. After left frontal craniotomy, transcortical approach was done. Total removal was accomplished and the postoperative course was uneventful. GCMs do not seem differ clinically, surgically or histopathologically from small cavernous angiomas, but imaging appearance of GCMs may be variable. The clinical, radiological feature and management of GCMs are described based on pertinent literature review.