• 제목/요약/키워드: local recurrence

검색결과 800건 처리시간 0.021초

후두개에 발생한 방선균 감염 1례 (Actinomycotic Infection of the Epiglottis: A Case Report and Review)

  • 정승원;김경래;태경;김윤정
    • 대한기관식도과학회지
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    • 제16권2호
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    • pp.154-156
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    • 2010
  • We report a case of actinomycotic infection in epiglottis. Actinomycosis in the head and neck area is relatively rare but extremely rare in the larynx. A 63-year old man presented with continuous discomfort of the throat while swallowing. He had a history of oral injury caused by a fish bone a few weeks prior. Upon Examination with a flexible laryngoscope, a whitish round mass was noted at the lingual surface of the epiglottis. Under local anesthesia, a punch biopsy was performed and showed the typical features of actinomycosis. The mass was removed using a Diode laser under suspension laryngoscope. Additive oral antibiotic therapy was done for 2 weeks. No definite recurrence was noted at the operation site and the patient is now free of disease.

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동종골 이식술로 치료한 경골 근위부에 발생한 연골 육종 - 증례 보고 - (Chondrosarcoma of Proximal Tibia Trated by Allograft - A Case Report -)

  • 정구희;김재도;정소학;차상원
    • 대한골관절종양학회지
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    • 제12권2호
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    • pp.165-170
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    • 2006
  • 저자들은 근위 경골에 발생한 연골 육종 환자의 동종골 이식술을 이용한 수술적 치료후 만족할 만한 결과를 얻어 보고하고자 한다. 자기 공명 영상에서 종양의 크기는 $3.5{\times}20$ cm 이었고 적절한 수술연을 선택하여 광범위 절제술을 시행하였으며 결손부는 동종 골이식술 및 내측 비복근 회전 피판술 및 부분 층 피부 이식을 통하여 재건하였다. 최종 추시일 까지 국소 재발이나 원격 전이는 관찰 되지 않았으며 이차 감염이나 불유합, 금속물의 해리 등의 합병증도 발생하지 않았다. 또한 적절한 재활 운동을 통해 만족할 만한 슬관절 관절 운동을 얻을 수 있었다.

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슬관절 주위에 발생한 연부조직 골육종 - 증례 보고 - (Extraskeletal Osteosarcoma Around the Knee Joint - A Case Report -)

  • 이봉진;김태호;하창원;김성수
    • 대한골관절종양학회지
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    • 제15권1호
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    • pp.81-86
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    • 2009
  • 연부조직에 발생되는 골육종은 매우 드문 종양으로, 세계적으로 소수의 예가 보고되었으며 한국에서는 2례가 보고되었을 뿐이다. 문헌상 세계에서 최고령의 증례인 91 세 남자에서 외상, 방사선 조사, 화골성 근염, 피부 근염 등과 관련없이 슬관절 주위에 발생한 연부조직 골육종을 경험하였다. 절제술만으로 치료하였으며, 환자는 수술 후 1년 추시 상 생존해 있고 국소재발이나 전이의 징후가 없으며 슬관절의 기능도 양호한 상태이다.

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Sinus Tract Formation with Chronic Inflammatory Cystic Mass after Beta Tricalcium Phosphate Insertion

  • Kim, Hong Jin;Na, Woong Gyu;Jung, Sung Won;Koh, Sung Hoon;Lim, Hyoseob
    • 대한두개안면성형외과학회지
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    • 제18권4호
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    • pp.282-286
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    • 2017
  • Beta tricalcium phosphate (${\beta}-TCP$) is one of allogenic bone substitute which is known to have interconnected pores that draws cell and nutrients for bone generation. It has been resulted in good outcomes for bone defect coverage or augmentation. However, several studies have also reported negative outcomes and associated complications including unexpected formation of cystic mass, continuous pain and secretion. We present the case of a 36-year-old man with a right cheek cystic mass who had a history of right zygomaticomaxillary (ZM) complex fracture and surgical correction with ${\beta}-TCP$ powder insertion to ZM bone defect. Excisional biopsy under local anesthesia revealed calcified mass in a sinus tract which was found to be connected to the ZM bone defect site in postoperative computed tomography image. Further excision under general anesthesia was performed to remove the sinus tract and fine granules which filled the original defect site. Pathologic report revealed bony spicules and calcification materials with chronic foreign body reaction. Postoperative complications and recurrence were not reported.

Dual vascular free transverse rectus abdominis myocutaneous flap for hemifacial reconstruction in a vessel-depleted neck

  • Lee, Su-Hyun;You, Hi-Jin;Lee, Yun-Hwan;Kim, Deok-Woo
    • Archives of Plastic Surgery
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    • 제47권1호
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    • pp.88-91
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    • 2020
  • Cutaneous squamous cell carcinoma (SCC) is the second most common skin malignancy. This report describes the case of an unusual extensive SCC involving the whole hemiface, which required reconstruction with a combination of a dual vascular free transverse rectus abdominis muscle (TRAM) flap and a skin graft. A 79-year-old woman visited our hospital with multiple large ulcerated erythematous patches on her right hemiface, including the parieto-temporal scalp, bulbar and palpebral conjunctiva, cheek, and lip. A preliminary multifocal biopsy was performed in order to determine the resection margin, and the lesion was resected en bloc. Orbital exenteration was also performed. A free TRAM flap was harvested with preserved bilateral pedicles and was anastomosed with a single superior thyroidal vessel. The entire TRAM flap survived. The final pathological examination of the resected specimen confirmed that there was no regional nodal metastasis, perineural invasion, or lymphovascular involvement. The patient was observed for 6 months, and there was no evidence of local recurrence. Usage of a TRAM flap is appropriate for hemifacial reconstruction because the skin of the abdomen matches the color and pliability of the face. Furthermore, we found that the independent attachment of two extra-flap anastomoses to a single recipient vessel can safely result in survival of the flap.

두피에 발생한 거대 표피모반 치험례 (A Case Report of a Giant Epidermal Nevus on the Scalp)

  • 배인호;은석찬;백롱민
    • 대한두개안면성형외과학회지
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    • 제12권1호
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    • pp.67-70
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    • 2011
  • Purpose: Epidermal nevi are hamartomas of the skin with multiple clinical variants. Normally, epidermal nevi present at an early age, are found on the head and neck area, and have a female predominance. Only very rarely do epidermal nevi have an adult onset. Most lesions are small and giant Epidermal nevi (> 5 cm at its greatest diameter) are quite rare. Huge verrucous plaque was observed on the scalp of a 70-year-old man. He had been reclusive for a long time, and this problem might have played a crucial role in the development of the giant epidermal nevi. Methods: A punch biopsy and MRI imaging were performed. The huge mass was resected. A local flap and split thickness skin graft was used for reconstruction. Results: The histology examination revealed the characteristic findings of epidermal nevus. Postoperatively, the patient did not suffer from complications or recurrence. Conclusion: A rare case of a huge epidermal nevus on the scalp of an elderly man was treated with a surgical excision. This is the oldest patient reported with an adult onset epidermal nevus in Korea.

설배부에 발생한 연골성분리종 1례 (A Case of Chondroid Choristoma on the Dorsum of the Tongue)

  • 길부관;손호진;김보문;정재원;김정규
    • 대한두경부종양학회지
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    • 제34권2호
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    • pp.43-46
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    • 2018
  • Chondroid choristomais a rare tumor like lesion of normal tissue in an unusual location. Oral cavity chondroid choristoma is exceedingly uncommon. This lesion is commonly covered by normal oral mucosa and can develop during a whole lifetime. We experienced a case of 57-year-old man who presented as 6-months history of asymptomatic mass on the dorsal surface of the tongue. We performed surgical excision under local anesthesia, and the pathological diagnosis was chondroid choristoma. After surgery, patient was followed up without any recurrence and discomfort. Therefore, we report this case with a review of literature.

갑상선 유두암 원주세포변형 1예 (A Case of Columnar Cell Variant of Papillary Thyroid Carcinoma)

  • 최시홍;이동후;정수진;김도훈
    • 임상이비인후과
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    • 제29권2호
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    • pp.281-285
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    • 2018
  • Columnar cell variant of papillary thyroid carcinoma (CCV-PTC) is a rare variant representing 0.15-0.2% of all PTCs. The CCV is aggressive, due to its rapid growth, high local recurrence rate, and frequent lung, brain and bone metastasis. Aggressive surgical and medical management are recommended for these neoplasias. The authors experienced a case of CCV-PTC in a 45-year-old man. We performed total thyroidectomy with neck dissection. The patient received radiation and radioactive iodine therapy. There were no recurrences or complications in the following 24 months after the operation. The patient will closely undergo continuous follow up. We present the clinical characteristics, pathology, treatment, and prognosis of the tumor with a review of the literature.

Intramuscular hemangioma in the zygomaticus minor muscle: a case report and literature review

  • Wee, Sung Jae;Park, Myong Chul;Chung, Chan Min;Tak, Seung Wan
    • 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.

Removal of intraosseous hemangioma in frontal bone under direct vision through a small incision

  • Kim, Hyeon Seok;Kim, Woo Seob;Kim, Han Koo;Bae, Tae Hui
    • 대한두개안면성형외과학회지
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    • 제22권1호
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    • pp.52-55
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    • 2021
  • Complete surgical excision within a margin of normal healthy bone is the treatment of choice for intraosseous hemangioma. A 56-year-old man visited with complaints of a firm, mildly tender, immovable, and palpable mass on the right forehead (size: 1.5×1.5 cm). Non-contrast brain computed tomography performed preoperatively revealed a 1.5 cm heterogenous osteolytic lesion with suspected internal trabeculation in the right frontal bone. Under general anesthesia, a 2 cm transverse incision was made on the forehead skin rather than bicoronal incision. Full-thickness en bloc resection of the frontal bone including the mass was performed. The frontal bone was removed with care taken not to damage the frontal sinus mucosa. The frontal sinus was sealed with a collagen patch (Tachocomb) and a cranioplasty was performed using bone cement. At 6 months postoperative, a clean wound was confirmed without any complications, and there was no local recurrence. Surgical excision of intraosseous hemangioma in the frontal sinus bone can be performed via direct incision or the bicoronal approach. In this case, the direct incision approach was used to achieve smaller scars and faster recovery than the bicoronal approach.