• Journal of Chest Surgery
• /
• 제43권2호
• /
• pp.208-211
• /
• 2010

종격동에 발생하는 혈관종은 전체 종격동 종양의 0.5% 이하로 드문 양성 질환이다. 이중 모세관혈관종과 해면혈관종이 90% 이상을 차지하고 정맥혈관종은 국내에선 보고된바 없으며 세계적으로도 보고된 예가 드물다. 44세 여자 환자가 대장암 수술 후 추적관찰을 위해 시행한 흉부 전산화 단층촬영상 종격동 종괴가 우연히 발견 되었다. 우리는 이를 고형체로 의심하고 종격 내시경하 조직검사를 시행하던 중 출혈이 발생하여 개흉술로 전환한 후 완전 절제한 정맥 혈관종을 경험하였기에 이를 보고하는 바이다.

• Journal of Chest Surgery
• /
• 제37권5호
• /
• pp.460-463
• /
• 2004

종격동에 발생한 혈관종은 전체 종격동 종양의 0.5% 미만을 차지할 정도로 드문 질환이다. 후종격동에 발생한 혈관종의 경우는 전종격동에 비해 더 드문 것으로 알려져 있다. 환자는 21세 여자로 단순흉부 방사선촬영상 후종격동에 비정상적인 음영을 보여 본원으로 전원되어 시행한 흉부 전산화 단층촬영과 흉추 자기공명 영상촬영에서 척수 경막까지 도달되어 있는 아령모양의 후종격동 종양 소견을 보였다. 이에 수술적 절제를 시행하였고 병리 조직학적 검사결과 3${\times}$4${\times}$2 cm의 모세혈관상 혈관종의 소견이 관찰되었다.

• Journal of Chest Surgery
• /
• 제34권5호
• /
• pp.410-413
• /
• 2001

심장에서 발생하는 모셀혈관종은 극히 드문 양성 종양이다. 본원에서는 호흡곤란을 주소로 내원한 13세 남자 환자에서,심포음파상 중등도의 혈류 폐쇄를 초래하는 우심실내 종괴를 확인한 후, 우심방을 통해 완전 절제하여 조직검사상 모세 혈관종을 발견하였기에 문헌고찰과 더불어 증례보고하는 바이다.

• 대한후두음성언어의학회지
• /
• 제21권2호
• /
• pp.139-141
• /
• 2010

Pyogenic granuloma in larynx is very rare. It is benign disease, and histopathologically it looks like capillary-rich hemangioma. The most common etiology of pyogenic granuloma is laryngeal trauma, usually related to intubation. It can be treated with speech therapy, medication, or surgical resection. We experienced a case of large pyogenic granuloma in larynx with feeding vessels of a 24-year-old woman. When she visited us, she suffered from dyspnea. We had performed excision of laryngeal mass by laryngeal microsurgery emergently. She was diagnosed with pyogenic granuloma in larynx after operation.

• 대한구순구개열학회지
• /
• 제13권2호
• /
• pp.85-92
• /
• 2010

Vascular malformations (VMs) in the head and neck region are present at birth and grow commensurately with the child, they can result in significant cosmetic problems for the patient, and some may lead to even serious life threatening hemorrhage. Although the molecular mechanisms underlying the formation of these VMs remain unclear, lesions are known to result from abnormal development and morphogenesis. Histologically, there are no evidence of cellular proliferation, but rather progressive dilatation of abnormal channels, which VMs are designated to their prominent channel types such as capillary, venous, lymphatic, arterial, and combined malformations. VMs with an arterial component are rheologically fast-flow, whereas capillary, lymphatic, and venous components are slow-flow. In this article, we review the clinical presentations, diagnosis, and management of VMs of facial regions with author's embolization and surgical treatment cases.

• Archives of Plastic Surgery
• /
• 제43권1호
• /
• pp.19-25
• /
• 2016

Background The vermilion plays an important role in both the aesthetic and functional aspects of facial anatomy. Due to its structural features, the complete excision of vascular anomalies on the vermilion is challenging, making it difficult to determine the appropriate treatment strategy. Thus, the authors analyzed the results of surgical treatment of vascular anomalies on the vermilion. Methods The medical records of 38 patients with vascular anomalies on the vermilion who underwent surgery from 1995 to 2013 were analyzed. Nine of the cases had an involuted hemangioma, and 29 cases had a vascular malformation; of the vascular malformations, 13, 11, one, and four cases involved were capillary malformations (CMs), venous malformations (VMs), lymphatic malformations (LMs), and arteriovenous malformations (AVMs), respectively. We investigated the surgical methods used to treat these patients, the quantity of surgical procedures, complications and instances of recurrence, and self-assessed satisfaction scores. Results A total of 50 operations were carried out: 28 horizontal partial excisions, eight vertical partial excisions, and 14 operations using other surgical methods. All cases of AVM underwent complete excision. Six cases experienced minor complications and one case of recurrence was observed. The overall average satisfaction score was 4.1 out of 5, while the satisfaction scores associated with each lesion type were 4.2 for hemangiomas, 3.9 for CMs, 4.2 for VMs, 5.0 for LMs, and 4.0 for AVMs. Conclusions It is difficult to completely excise vascular anomalies that involve the vermilion. This study suggests that partial excision focused on correcting the overall contour of the lips is effective and leads to satisfactory results.

• Archives of Hand and Microsurgery
• /
• 제23권4호
• /
• pp.301-305
• /
• 2018

혈관종은 내피세포로부터 기원한 양성종양의 일종으로, 수부에서는 드물게 발생하는 것으로 알려져 있다. 62세 여자환자로 우측 2수지 요골측의 통증을 주소로 내원하였으며, 시행한 자기공명영상에서 수지신경을 압박하는 것으로 보이는 혈관종이 의심되었다. 수술을 시행하여 요골측 수지신경 및 수지혈관을 압박하고 있는 혈관종을 확인하였으며, 수지신경 및 혈관을 가능한 보존하기 위하여 미세수술을 통해 혈관종을 제거하였다. 공간점유성 병변에 의한 압박성 신경병증은 드문 일로, 정확한 진단에 어려움이 있으나, 본 증례와 같이 자기공명영상을 통한 술 전 평가와 및 미세수술을 이용한 병변 제거 및 신경 보존을 통하여 신경병성 통증을 성공적으로 호전시킬 수 있을 것으로 생각한다.

• Journal of Korean Neurosurgical Society
• /
• 제44권2호
• /
• pp.72-77
• /
• 2008

Objective : The objective of this study was to evaluate the characteristics and surgical outcome of the conus medullaris tumors. Methods : We retrospectively reviewed 26 patients who underwent surgery for conus medullaris tumor from August 1986 to July 2007. We analyzed clinical manifestation, preoperative MRI findings, extent of surgical resection, histopathologic type, adjuvant therapy, and outcomes. Results : There were ependymoma (13), hemangioblastoma (3), lipoma (3), astrocytoma (3), primitive neuroectodermal tumor (PNET) (2), mature teratoma (1), and capillary hemangioma (1) on histopathologic type. Leg pain was the most common symptom and was seen in 80.8% of patients. Pain or sensory change in the saddle area was seen in 50% of patients and 2 patients had severe pain in the perineum and genitalia. Gross total or complete tumor resection was obtained in 80.8% of patients. On surgical outcome. modified JOA score worsened in 26.9% of patients, improved in 34.6%, and remained stable in 38.5%. The mean VAS score was improved from 5.4 to 1.8 among 21 patients who had lower back pain and leg pain. Conclusion : The surgical outcome of conus medullaris tumor mainly depends on preoperative neurological condition and pathological type. The surgical treatment of conus medullaris tumor needs understanding the anatomical and functional characteristics of conus meudllaris tumor for better outcome.

• 대한통합의학회지
• /
• 제9권4호
• /
• pp.85-89
• /
• 2021

Background : Klippel-Trenaunay-Weber syndrome (KTS) is a rare congenital medical condition characterized by complex vascular malformation. KTS consists of a classic triad of capillary malformation (hemangioma), venous malformations and bone or soft tissue hypertrophy causing limb asymmetry. The aim of this report is to describe management for gait disturbance and foot pain in a Patient with KTS using custom-made total contact insole. Case presentation : A 32-year-old man with KTS presented with a 3-year history of gait disturbance on hard surface due to right first toe pain and Achilles tendon tightness. The patient had soft tissue hypertrophy, varicose veins and port-wine stains over the right lower limb associated with KTS. True leg length discrepancy was 2 cm. We prescribed custom-made total contact insole to protect his deformed foot and correct leg length discrepancy. The insole of right side included wedge shaped heel lift and the insole of left side included full length lift to add extra support on unaffected side. Also, we provided compression stocking and physiotherapy including manual lymphatic drainage for lymphedema and stretching exercise for tightness in right lower extremity. At 3 years follow-up, postural alignment including pelvic obliquity was improved using a custom-made total contact insole. The degree of scoliosis and foot pain were also reduced. Conclusion : An individualized and multidisciplinary approach is essential regarding the complexity of comorbidities in patients with KTS. For patients with KTS, orthotic management should be considered to prevent and correct deformities related to KTS. Active orthotic management, compression stocking and physiotherapy can enhance the quality of life and function in patients.

• 대한골관절종양학회지
• /
• 제8권3호
• /
• pp.76-82
• /
• 2002

목적: 거골 체부에 발생하는 양성 종양은 매우 드물어 치료 방법에 따른 결과를 비교하기 어렵다. 이 연구에서는 거골 체부에 발생한 양성 종양 8예를 후방 도달법과 후 돌기를 통한 소파술로 치료한 결과를 보고하고자 한다. 대상 및 방법: 1986년 2월부터 2001년 8월 사이에 저자들이 경험한 거골 체부에 발생한 양성 골종양 환자 8명을 연구 대상으로 하였다. 종양의 발견 당시 평균 연령은 22.1세(10세~41세)이었고, 남자 4명, 여자 4명이었다. 종양의 종류는 거대세포종 2례, 유골 골종 2례, 연골모세포종 1례, 골내 모세혈관종 1례, 단순 골 낭종 1례, 골연골종 1례이었다. 모두 후방도달 법으로 접근하였고, 2례의 유골 골종과 1례의 골연골종 환자는 절제술을, 나머지 5례는 후 돌기를 통한 소파술을 시행하였다. 평균 추시 기간은 7.5년(1년~16년)이었다. 결과: 추시 기간 중에 재발한 환자는 없었고, 1례에서 감염증이 발생했다. 이 경우를 제외한 모든 경우에서 체중 부하시 통증은 없었고, 관절 운동 범위의 제한이 발생한 경우도 없었다. 결론: 거골 체부에 발생한 양성 종양은 후방 도달법으로 주위 조직의 손상 없이 안전하게 접근할 수 있으며, 거골의 후 돌기를 통한 피질골 창으로 만족할 만한 소파술이 가능함을 알 수 있었다.