• Journal of Chest Surgery
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• 제47권2호
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• pp.149-151
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• 2014

Hemangioma of the heart, presenting as a primary cardiac tumor is extremely rare; it accounts for approximately 2% of all primary resected heart tumors. In our patient, the tumor was located in the orifice of the right lower pulmonary vein. Few cases of cardiac hemangiomas have been reported to arise from the left atrial (LA) wall. Left atrial hemangiomas, especially those attached to the LA wall, may be erroneously diagnosed as myxomas. Cardiac hemangioma is a rare disease; furthermore, a tumor arising from the LA wall and misconceived as a myxoma is extremely rare. We removed a mass misdiagnosed as a myxoma; it was pathologically confirmed to be a cardiac capillary hemangioma. Therefore, we report a rare case of a cardiac hemangioma misconceived as a myxoma; the tumor was removed successfully.

• Neonatal Medicine
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• 제17권1호
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• pp.116-122
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• 2010

Kasabach-Merritt 증후군은 거대한 혈관종에 의해 혈소판이 소모되어 감소되는 드문 질환이다. 저자들은 재태주령 32주 미숙아에서 설명되지 않은 복수와 혈소판 감소증의 원인을 찾기 위해 시험적 개복술을 시행하여 장 혈관종을 발견하였으나 광범위하여 수술적 제거를 하지 못하고, SPECT로 확인 후 스테로이드 치료로 혈소판 감소증이 호전된 1례를 경험하였다. 따라서 다른 원인에 의해 설명되지 않는 혈소판 감소증과 파종성 혈관내 응고병증이 있으면 내부 장기의 혈관종을 의심해 볼 필요가 있다고 사료되었다.

• Journal of Chest Surgery
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• 제32권9호
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• pp.851-854
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• 1999

식도에서 발생한 혈관종은 전 세계적으로 30례 정도가 보고된 매우 드문 질환이다. 일반적으로 남자에 서 흔하고 증상이 없는 경우가 대부분이나, 연하 곤란 및 출혈 등이 있을 수 있다. 진단은 바륨 식도 조 영술과 내시경을 통해 이루어지고, 치료 방법은 내시경적 절제술과 개흉을 통한 절제술이 있다. 환자는 연하 곤란과 소화 불량을 주소로 내원한 46세 남자로 식도 조영술, 내시경 검사상 식도 중하부의 점막하 종양이 추정되어 수술을 시행하였다. 개흉수술을 통해 절제하였고 조직 검사상 해면상 혈관종으로 확진 되었다. 수술후 합병증이 없이 퇴원하였으며 수술후 관찰 추적중인데, 재발없이 양호한 상태를 보이고 있다.

• 대한두개안면성형외과학회지
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• 제22권2호
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• pp.115-118
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• 2021

Intramuscular hemangioma is a rare vascular benign proliferation that can occur within any muscle, particularly in the trunk and extremities. In the head and neck region, the masseter muscle is most commonly involved, followed by the periorbital and sternocleidomastoid muscles. Diagnosing intramuscular hemangioma is challenging because there are no characteristic symptoms; instead, magnetic resonance imaging is the best imaging modality to diagnose these lesions. Complete surgical resection is the treatment of choice, although the local recurrence rate is high. Herein, we report a rare case of intramuscular hemangioma located in the zygomaticus minor muscle, which is related to smiling and usually runs along the orbicularis oculi muscle. Distinguishing or separating these two muscles is challenging. However, based on the muscle vector of the midface and radiological findings, the two muscles were successfully separated. The zygomaticus minor was cut very slightly to approach to the lesion and the muscle fibers were split to excise it. A follow-up examination revealed no nerve damage or muscle dysfunction at 4 weeks postoperatively. This rare case may serve as a reference for managing intramuscular hemangioma in the head and neck region.

• 대한후두음성언어의학회지
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• 제32권2호
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• pp.104-108
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• 2021

The etiology of laryngeal hemangioma is unclear, and it is classified into infant and adult types. The former is capillary hemangioma and relatively common, the latter is cavernous type and very rare. The adult laryngeal hemangioma mainly occurs in supraglottis and glottis. A 75-year-old man came to our clinic with a voice change that started four months ago. The laryngoscopic finding showed that the surface of oval-shaped mass is covered with turbid exudates. We performed the laryngeal microsurgery with CO₂ laser. The mass was pathologically proven as cavernous hemangioma. We report a very rare and didactic case with review of relevant literature.

• Tuberculosis and Respiratory Diseases
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• 제47권5호
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• pp.704-708
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• 1999

저자들은 대량객혈을 주소로 입원한 32세 여자 환자에서 기관하부에 종괴를 발견하고, 종괴자체로 인한 호흡곤란이나 기도폐쇄 소견없이 단지 재발하는 객혈이 문제되어 기관내로 내시경적 처치가 가능하고 광선 응고효과가 뛰어난 Nd:YAG 레이저를 사용하여 치유한 기관 혈관종 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

• 대한관절경학회지
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• 제10권1호
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• pp.91-94
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• 2006

활액막 혈관종은 주로 소아나 젊은 연령의 성인에게 발생하며 동통, 운동제한 및 혈관절증을 유발하는 드문 양성종양으로 슬관절에 가장 호발한다. 혈슬관절증으로 내원한 39세 여자 환자에서 관절내 활액막 혈관종을 순수 관절경 시야 하에서 절제한 증례를 바탕으로 하여 활액막 혈관종의 진단과 치료에 대해 검토해 보고자 한다.

• Clinics in Shoulder and Elbow
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• 제17권4호
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• pp.185-189
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• 2014

We report a case of intramuscular hemangioma in the subscapularis muscle and the resulting impairment of shoulder function in an adult patient. A nineteen-year-old female complained of shoulder pain and the development of a mass in the absence of previous trauma. Physical examinations, including lift-off and belly-press tests, showed abnormality. X-ray showed multiple calcifications in the front of the scapula. Magnetic resonance imaging showed a soft-tissue mass occupying almost the entire intramuscular portion of the subscapularis muscle. An arthroscopic examination excluded the possibility of a joint invasion, after which the entire mass was successfully removed by open excision. The displacement of the subscapularis by the mass was relieved after the surgery. Pathological diagnosis of the tissue confirmed a cavernous hemangioma. Both shoulder pain and function was improved after operation. There was no evidence of recurrence even at the 2-year follow-up. Rare forms of hemangioma adjacent to the shoulder joint could be successfully managed with surgical excision. Differential diagnosis, such as synovial chondromatosis, pigmented villo-nodular synovitis, and malignant sarcoma, should also be considered.

• Tuberculosis and Respiratory Diseases
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• 제75권1호
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• pp.36-39
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• 2013

Capillary hemangioma of the tracheobronchial tree is an extremely rare benign tumor in adults, especially those located in the bronchus. Characteristics and treatment of capillary hemangiomas of adult tracheobronchial trees have not been well known. We present a 61-year-old man with hemoptysis, which was caused by a small tiny nodule in the left lingular segmental bronchus. The nodule was removed by a forcep biopsy, via flexible bronchoscopy, and it was revealed to be capillary hemangioma. A small isolated endobronchial capillary hemangioma can be treated with excisional forcep biopsy, but a risk of massive bleeding should not be overlooked.

• 대한골관절종양학회지
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• 제16권1호
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• pp.37-41
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• 2010

골성 골단에서 발생하는 혈관종은 극히 드물어서 그 보고를 찾아보기가 쉽지 않다. 우측 슬관절부 동통과 굴곡 구축을 주소로 내원한 5세 환아로 단순 방사선 및 자기공명영상 소견상, 대퇴골 원위부 골단 및 근위부 경골에서 병변을 보였으며, 생검한 결과 혈관종으로 진단되었다. 8년간 추시 관찰하였으며, 대퇴골 원위부 골단에 발생한 혈관종은 치유되었으며, 경골 근위부 골단에 발생한 병변도 치료없이 자연적으로 소실되었다. 또한, 하지 길이의 단축이나 슬관절 기능 장애는 발생하지 않았다.