• 제목/요약/키워드: Surgical curettage

검색결과 86건 처리시간 0.019초

족부, 족관절 결핵 (Tuberculosis in Foot and Ankle)

  • 최장석;곽희철;김정한;정훈재
    • 대한족부족관절학회지
    • /
    • 제12권2호
    • /
    • pp.203-209
    • /
    • 2008
  • Purpose: To emphasize the importance of considering tuberculosis in atypical cases of foot and ankle by reporting clinical results of those cases. Materials and Methods: Seven cases which were diagnosed as tuberculosis around foot and ankle from March 1996 to June 2007 were included. We reviewed initial impressions, the time to be diagnosed, clinical symptoms, laboratory findings, radiological findings and the clinical results and complications. Results: We followed up at least 6 months ($6{\sim}24$ months) after surgery in all cases. Initially 2 cases had been diagnosed as cellulitis, 4 cases as chronic osteomyelitis, and 1 case as an ankle instability. Tuberculosis was diagnosed after biopsy in all cases. Mean duration of symptom was 15 months ($6{\sim}36$ months) except in infants. There were various radiologic manifestations such as osteopenia, bony erosion or destruction and cystic changes. Symptoms were relieved in all cases within 4 months with chemotherapy followed by surgical biopsy, except one ankle which had been misdiagnosed as ankle instability and joint destruction was developed after modified Brostrom surgery. Conclusion: It is important to perform a surgical biopsy for diagnosis and proper management even with a faint suspicion on tuberculosis in foot and ankle. And in case of need, when surgical biopsy is performed, curettage procedure may help to improve clinical result.

  • PDF

경부 결핵성 임파선염의 임상적 고찰 (Clinical analysis of tuberculous cervical lymphadenitis)

  • 김영민;송병찬;윤성철;박영민
    • 대한기관식도과학회:학술대회논문집
    • /
    • 대한기관식도과학회 1993년도 제27차 학술대회 초록집
    • /
    • pp.107-107
    • /
    • 1993
  • 경부 결핵성 임파선염은 우리나라에서 경부 종괴의 흔한 원인중의 하나이다. 그러나 대부분 확진이 어려우며, 또한 효율적인 치료도 아직 논란이 많다. 저자들은 1989년 6월부터 1993년 2월까지 약 4년간 한림대학부속 강남성심병원에 경부종괴로 내원하여 수술적 치료를 시행하여 경부 결핵성 임파선염으로 확진되었던 32례에 대한 후향적 임상조사를 실시하여 경부 전산화단층촬영 소견을 5가지 유형으로 분류하였으며, 수술적 치료유형에 대한 고찰을 하여 다음과 같은 결과를 얻었다. 1. 종물의 위치는 후경부가 12례로 가장 많았으며 하악부 9례, 쇄골상부 8례, 이하부 2례, 이하선부 1례이었다. 2, 경부 전산화단층촬영 소견에 따라 다음의 5가지 형태로 분류할 수 있었다. : 균등조영 증강형 3례, 변연조영증강형 6례, 주변유착형 12례, 농양형 8례, 혼합형 3례. 3. 수술적 치료는 종물 절제술 13례, 절개 및 배농 9례, 선택적 경부청소술 8례, 소파술 2례를 시행하여 만족스러운 결과를 얻었다.

  • PDF

안면부에 발생한 각화극세포종의 치험례 (KERATOACANTHOMA ON FACIAL SKIN : CASE REPORT)

  • 강희인;이원학;오해수;김동석;김상중
    • Maxillofacial Plastic and Reconstructive Surgery
    • /
    • 제27권6호
    • /
    • pp.570-574
    • /
    • 2005
  • Keratoacanthoma is a benign, self-limited epithelial lesion that closely resembles Squamous cell carcinoma(SCC). Keratoacanthoma occur primarily exposed skin in male patients over 45 years of ages. although etiology is unknown, sunlight, genetic, and human papillomavirus factor have been considered. in clinical feature, rapid enlargement occurs over 4$\sim$8 weeks, resulting ultimately in a hemispheric, firm, elevated, asymptomatic nodule that contains a central plug of keratin. When fully developed, the keratoacanthoma contains a core of keratin surrounded by a concentric collar of raised skin. Over the next 4$\sim$8 weeks, static lesion persists. Then undergoes spontaneous regression over the next 6$\sim$8weeks period by expulsion of the keratin core with resorption of the mass. In histologic feature, Keratoacanthoma consists of hyperplastic squamous epithelium growing into the underlying connective tissue. The surface is covered by a thickened layer of parakeratin with central plugging. Epithelium cell shows dysplastic features and the margins the normal adjacent epithelium is elevated. The differential diagnosis includes SCC. Keratoacanthoma present as a exophytic lesion with horny keratin occupying a depression on the top of the lesion, persists static period and undergoes rapid growth compared with SCC. Keratoacanthoma is usually treated by surgical excision or curettage of the base, spontaneous regression does not occur in every case. A 60 years old male who present facial lesion visit our hospital and surgical excision was done. Biopsy result was keratoacanthoma. We report case with review of literatures.

소아에서 둔부 근육주사 후 발생한 국소 합병증 (Local Complications after Intramuscular Buttock Injections in Children)

  • 박두현;이남혁;김상윤
    • Advances in pediatric surgery
    • /
    • 제4권2호
    • /
    • pp.137-143
    • /
    • 1998
  • Intramuscular injection(IM) into the gluteal muscles is a common route of medication, but may lead to complications. A retrospective review of 32 patients who required surgical treatment for local complications of buttock injections in children was made at the Taegu Fatima Hospital during a seven-year nine-month period (March 1990 to December 1997). Local complications included acute inflammation, cellulitis and abscess(71.9 %), and fat necrosis(21.9 %), and injection granuloma(6.2 %). Over the half of injections were on the upper and outer quadrant of the buttock, but the other 43.7 % were in the upper and inner or lower and outer quadrant which are considered unsuitable sites for intramuscular injection. The majority of complications developed within fat tissue(90.6 %) rather than within muscle(9.4 %). Two-thirds of the patients were under 2 years of age, this suggests that it is technically difficult to accurately administer IM injections in small children because muscle mass is smaller compared to subcutaneous. In addition subcutaneous fat is more susceptible to chemical irritation. Staph. aureus was the predominant organism, isolated in 84.6 % of the patients with abscesses. Treatment consisted of needle aspiration, incision and drainage, curettage, or surgical excision. In conclusion, the major factor that contributes to complications following IM of the buttock appears to be the inadvertent intrafat rather than of IM injection. Accurate injection into the muscles based on a knowledge of pelvic anatomy as well as the potential complications is necessary to prevent complications.

  • PDF

우측 측두골에 재발한 연골아세포종의 증례보고 (RECURRENT CHONDROBLASTOMA ON THE RIGHT TEMPORAL AREA : A CASE REPORT)

  • 서운경;허필우;이원;김성훈;고택수;허현아;김인수
    • Maxillofacial Plastic and Reconstructive Surgery
    • /
    • 제27권4호
    • /
    • pp.388-393
    • /
    • 2005
  • Chondroblastoma was introduced as a rare benign cartilaginous neoplasm by Codman in 1931. It described by Jaffe and Lichtenstein in 1942 as a benign cartilaginous neoplasm that represents less than 1% of all primary bone tumor. It commonly arises in the epiphysis of long bone but, it occurs very rare in temporal area. Sometimes, microscopic identification of chondroblastoma and giant cell granuloma is difficult. An immunohistochemical studies was performed for S-100 protein which is useful in arriving at the correct diagnosis. Treatment modalities are total curettage, en-bloc excision, irradiation, and radiation combined with surgical excision. But radiation therapy was controversial. We describe a case of chondroblastoma which was arisen in the right temporal area and the recurrence that was treated by surgical excision and radiation therapy with review of literature.

Treatment and Rehabilitation of Repetitively Recurrent Langerhans Cell Histiocytosis: A Case Report

  • Yoo, Hee Young;Park, Kyung Soo;Lee, Baek Soo;Kwon, Yong Dae;Choi, Byung Joon;Ohe, Joo Young;Lee, Jung Woo
    • Journal of Korean Dental Science
    • /
    • 제9권1호
    • /
    • pp.35-41
    • /
    • 2016
  • Langerhans cell histiocytosis (LCH) is characterized by proliferation of histiocyte-like cells (Langerhans cell histiocytes) with characteristic Birbeck granules, accompanied by other inflammatory cells. Treatments of LCH include surgery, chemotherapy, and radiotherapy. One of the representative forms of chemotherapy is intralesional injection of steroids. Surgical treatment in the form of simple excision, curettage, or even ostectomy can be performed depending on the extent of involvement. Radiotherapy is suggested in case of local recurrence, or a widespread lesion. This article shows the case of repetitively recurrent LCH of a 56-year-old man who had been through surgical excision and had to have marginal mandibulectomy and radiotherapy when the disease recurred. After the first recurrence occurred, lesions involved the extensive part of the mandible causing pathologic fracture, so partial mandibular bone resection was performed from the right molar area to the left molar area followed by the excision of the surrounding infected soft tissues. The resected mandibular bone was reconstructed with a segment of fibula osteomyocutaneous free flap and overdenture prosthesis supported by osseointegrated implants.

하악 제3대구치 발치 시 합병증으로 발생할 수 있는 악하선과 설신경 손상: 증례보고 (Injury of submandibular gland and lingual nerve as complication third molar tooth extraction in mandible : a case report)

  • 임재성;윤현중;이상화
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
    • /
    • 제37권2호
    • /
    • pp.137-141
    • /
    • 2011
  • The extraction of an impacted third molar tooth is associated with many complications during the procedure and postoperative care. These complications include bleeding, swelling, pain, infection, as well as root fracture, proximal tooth injury, alveolar bone fracture, lingual nerve and inferior alveolar nerve injury etc. With the exception of a fractured root dislocation in the submandibular space, no direct submandibular gland injury related to extraction surgery has been reported until now. A 40 year old man visited the department of oromaxillofacial surgery at Yeouido St. Mary's Hospital for an extraction of the right mandible third molar. A partial third molar impaction was diagnosed by a clinical and radiographic examination. A surgical tooth extraction was practiced including buccal cortical bone osteotomy. During socket curettage, an encapsulated cyst-like lesion and a verified $3{\times}3\;cm$ neoplasm in the apically lingual direction were found during process of dissection. A biopsy confirmed that the neoplasm involved the submandibular gland and nerve trunk. This unusual anatomical organ injury during the surgical tooth extraction procedure is reported as a new complication during impacted third molar extraction.

하악 이부에 생긴 Angiolymphoid hyperplasia with eosinophilia(Kimura's disease)의 치험례 (THE CASE REPORT OF ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA ON CHIN)

  • 양윤석;조용석
    • Maxillofacial Plastic and Reconstructive Surgery
    • /
    • 제18권3호
    • /
    • pp.443-447
    • /
    • 1996
  • Angiolymphoid hyperplasia with eosinophilia(ALHE) is an uncommon, benign vascular proliferation with the background of a stroma which is heavily infiltrated by lymphocytes and eosinophils and includes lymphatic follicles with prominent germinal centers. ALHE primarily involves the skin and subcutis in head and neck as various forms of nodules. There has been considerable controversy about the relationship between ALHE and Kimura's disease. Kimura's disease, originally reported by Kimura et el., is an unusual granulation with proliferation of lymphoid tissue. Wells and Whimster published the first report describing a condition that resembled Kimura's disease and designated it as ALHE. For a time being two lesions are thought to be same lesion, but recently they are considered as two different entities, histopathologically. The cause of this disease remains unknown, and physicians have used a variety of treatment modalities including cryosurgery, steriod therapy, electrodesiccation, curettage, radiotherapy, laser therapy and surgical excision. But any treatment modality leaves problem of recurrence because the lesion is not well encapsulated. Being poorly encapsulated, the lesion's remnants are apt to be left and this markes some problems : recurrence and possible adjacent organ injury. In this case we misdiagnosed the lesion as well encapsulated benign mass. We performed excisional biopsy and experienced prolonged operation time and unwanted mentalis muscle injury. We think that the importance of poor encapsulation of ALHE should be stressed. So we report our experience with literature review.

  • PDF

핏불테리어 견에서 발생한 브로디씨 농양 (Brodie's Abscess in a Pit Bull Terrier Dog)

  • 최호정;이영원;왕지환;연성찬;이효종;이희천
    • 한국임상수의학회지
    • /
    • 제27권2호
    • /
    • pp.183-185
    • /
    • 2010
  • 3년령의 핏불테리어 견이 3주간의 좌측후지 파행을 주증상으로 내원하였다. 일반방사선검사상에서 경계명확한 골용해소견과 경계부위의 경화소견이 좌측 근위경골골간단의 내측면에서 관찰되었다. 수술적 소파술이 실시되었으며, Staphylococcus spp.가 수술중에 채취한 샘플의 배양결과 확인되었다. 이상의 검사결과를 바탕으로 브로디씨 농양으로 진단하였다.

개 상악에서 발생한 유두종성 에나멜아세포종과 섬유성 이형성의 병발 (Simultaneous Occurrence of an Acanthomatous Ameloblastoma and a Fibrous Dysplasia in the Maxilla of a Dog)

  • 정동인;예지영;서정향;왕지환;연성찬;이희천
    • 한국임상수의학회지
    • /
    • 제29권3호
    • /
    • pp.263-267
    • /
    • 2012
  • 4세령의 래브라도 리트리버견이 좌측상악의 종괴의 평가를 위해 내원하였다. 두개부 방사선학적 검사와 컴퓨터 단층촬영검사가 실시되었으며, 그 결과 좌측상악부의 골용해소견을 동반한 연부조직종괴가 확인되었다. 종괴의 적출과 소파술이 시행되었으며, 적출된 종괴는 조직병리학적 검사의뢰되었다. 조직병리학적 검사결과 섬유성 이형성이 동반된 유두종성 에나멜아세포종으로 진단되었다.