• 제목/요약/키워드: Life-threatening complication

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뇌 혈관계를 침범한 전신성 홍반성 루푸스 2례 (Two Cases of Systemic Lupus Erythematosus with Cerebrovascular Involvement)

  • 김봉준;이은영;홍영훈;박기도;송영두;이충기;심영란
    • Journal of Yeungnam Medical Science
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    • 제15권2호
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    • pp.371-380
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    • 1998
  • 저자들은 최근 루푸스가 뇌 혈관계를 침범하여 신경 정신과적 이상 증상을 보였으며 면역 검사, 뇌파 검사 및 뇌 자기공명사진에서 중추 신경 루푸스의 소견에 부합되는 양상을 보였고 고용량의 부신피질 호르몬 충격 요법에 반응이 좋았던 2례를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

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전신성 홍반성 루푸스 환자에서 발생한 괴사성 근막염의 치험례 (Necrotizing Fasciitis in a Patient with Systemic Lupus Erythematosus)

  • 조혜인;장학
    • Archives of Plastic Surgery
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    • 제38권3호
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    • pp.309-314
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    • 2011
  • Purpose: Necrotizing fasciitis is a life-threatening, destructive soft tissue infection with a very high rate of mortality that needs early diagnosis and aggressive treatment. Systemic Lupus Erythematosus (SLE) is a systemic, autoimmune disease and it's major cause of mortality is an infection. But necrotizing fasciitis in SLE is very rare and there have been only 22 cases reported in the literatures. We reported a patient of necrotizing fasciitis with SLE and reviewed 22 others from literature research. Methods: A 40-year-old female patient with a history of SLE for 6 years came to the emergency room. The patient complained of severe pain and swelling on her right leg. She was diagnosed as necrotizing fasciitis and underwent emergency fasciotomy. As wound cultures showed variable organisms, she was treated with broad-spectrum antibiotics and underwent several surgical debridements. Then, the wound was treated with the V.A.C (Vacuum Assisted Closure) device and split thickness skin grafting was performed two times. Results: Skin graft was well taken within 2 weeks after operations and the patient was discharged to outpatient follow up. There was no complication related with surgery and she could walk without cane after 3 months. Conclusion: We treated a necrotizing fasciitis in a patient with SLE and reviewed 22 others from literature research. The case presented here suggests that necrotizing fasciitis is a rare disease in SLE patients, but should be considered in the differential diagnosis of soft tissue infection in SLE patients. A high index of suspicion is needed for early diagnosis and proper management in these patients.

대상포진 후 발생한 비부의 괴사성 근막염 치험례 (Necrotizing Fasciitis of Nose Skin Following Herpes Zoster)

  • 배우식;배충상;노시균;이내호;양경무
    • 대한두개안면성형외과학회지
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    • 제13권2호
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    • pp.147-150
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    • 2012
  • Purpose: Varicella-zoster virus (VZV) infection is a common childhood disease. However, old and immune compromised patients are also at risk. Necrotizing fasciitis is a life threatening infection of the subcutaneous tissues, rapidly extending along the fascial planes. It is associated with a significant mortality rate, reported between 20% and 50%, and is therefore regarded as a surgical emergency. The authors treated a patient, who developed skin necrosis of her nose and left hemifacial area, following VZV infection. There are few literatures concerning this case; therefore, we present a rare case with review of literature. Methods: A 39-year-old woman had shown a localized, painful, multiple bullae and eschar formation in her nose and left hemifacial area for several days. Her skin lesion had rapidly worsened in size and morphology. Results: We diagnosed her as a necrotizing fasciitis, following herpes zoster, and then we performed a debridement of necrotic tissue and took a full thickness skin graft on her nose and left hemifacial area. Now, she was followed up with acceptable aesthetic result after 6 months. Conclusion: Secondary bacterial skin infection following VZV, can cause a result in a higher risk of complications. Among the complication, a necrotizing fasciitis of the head and neck is uncommon, and involvement of the nose is even more rare. Through this uncommon case report, we intend to emphasize the fact that early diagnosis of necrotizing fasciitis is very important, since it frequently necessitates surgical treatment which improves morbidity and leads to good recovery.

폐출혈을 동반한 현미경적 다발혈관염 1예 (A Case of Microscopic Polyangiitis with Diffuse Alveolar Hemorrhage)

  • 이상진;이재웅;김혜진;신경철;정진홍;이관호;박혜정
    • Journal of Yeungnam Medical Science
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    • 제21권1호
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    • pp.101-107
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    • 2004
  • Diffuse alveolar hemorrhage is a rare but serious and frequently life-threatening complication of a variety of conditions. The first goal in the management of patients with diffuse alveolar hemorrhage is to achieve or preserve stability of the respiratory status. Subsequently, the differential diagnosis is aimed at the identification of a remediable cause of the alveolar hemorrhage. The most common causes of diffuse alveolar hemorrhage with glomerulonephritis are microscopic polyangiitis and Wegener's granulomatosis, followed by Goodpasture syndrome and systemic lupus erythematosus. Microscopic polyangiitis (MPA) is a distinct systemic small vessle vasculitis affecting small sized vessels with few or no immune deposits and with no granulomatosus inflammation. The disease may involve multiple organs such as kidney, lung, skin, joint, muscle, gastrointestinal tract, eye, and nervous system. MPA is strongly associated with antineutrophil cytoplasmic autoantibody (ANCA) that is a useful serological diagnostic marker for the most common form of necrotizing vasculitis. Our report concerns a case of microscopic polyangiitis with diffuse alveolar hemorrhage in a 54-year-old man. He was admitted to our hospital due to dyspnea upon exertion and recurrent hemoptysis. Laboratory findings showed hematuria, proteinuria and deterioration of renal function. In the chest CT scan, diffuse ground glass appearance was seen in both lower lungs. A lung biopsy revealed small vessel vasculitis with intraalveolar hemorrhage and showed a positive reaction to against perinuclear ANCA. The patient was treated with prednisolone and cyclophosphamide. Chest infiltration decreased and hemoptysis and hypoxia improved. He is still being followed up in our hospital with a low dose of prednisolone.

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흉골 절개술 후 발생한 흉골 감염 및 종격동염의 Vacuum-assisted closure를 이용한 치료 - 3례 보고 - (Vacuum-Assisted Closure in Treatment of Poststernotomy Wound Infection and Mediastinitis - Three cases report -)

  • 장원호;허균;박영우;김현조;정윤섭;염욱
    • Journal of Chest Surgery
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    • 제35권2호
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    • pp.166-169
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    • 2002
  • 흉골 절개술 후 종격동염은 드물게 발생하나 심장 수술후 생명을 위협하는 합병증으로 발전할 수 있다. 지금까지는 흉골 절개술 후 발생한 창상 감염의 치료로서 창상세척과 변연 절개술 후 직접 상처 부위를 봉합하거나 근육 파판을 사용하여 왔다. 흉골 절개술 후 발생한 창상 감염의 새로운 치료로서 VAC(Vacuum-assisted closure) 술기에 대해 기술 하고자 한다. 이 술기를 흉골 절개술 후 발생한 창상감염 띤 종격동염 환자 3명에게 성공적으로 적용하였고, 이러한 새로운 방식으로 흉골 부위 상처를 치유할 수 있었다.

흉강경을 이용한 하행 괴사성 종격동염의 치료 (Management of Descending Necrotizing Mediastinitis with Thoracoscopy)

  • 이성호;선경;김광택
    • Journal of Chest Surgery
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    • 제35권2호
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    • pp.161-165
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    • 2002
  • 하행 괴사성 종격동염은 대부분 경부 부위의 농양으로 시작하여 종격동으로 파급되는 매우 치명적인 질환이며 저자에 따라 25∼40%의 사망률을 보고하고 있다. 빠른 진단과 적절한 수술적 치료가 중요하며 수술적 치료의 방법에는 아직 여러 가지 방법들이 보고되고 있지만 농양의 완전한 배농이 특히 중요하다고 보고하고 있다. 배농술은 경부 절개를 통한 배농과 함께 흉부 내의 종격동 배농술이 필요하며 종격동 배농술은 대부분 개흉술을 통하여 시행되어 왔으나 개흉술에 따른 합병증과 수술부위의 감염 등이 술후 이환율을 증가시키는 원인이 될 수 있다. 반면에 흥강경을 이용한 배농은 경부 배농술 및 흉부 배농술을 동시에 시행할 수 있으며 좋은 수술시야를 보여주고 술후 환자의 회복이 빨라 하행 괴사성 종격동염의 좋은 치료 방법이라 생각된다.

COL3A1 유전자의 새로운 돌연변이 c.2931+2dupT가 확인된 혈관형 엘러스-단로스 증후군 1례 (A Case of Vascular Ehlers-Danlos Syndrome with Novel Mutation c.2931+2dupT in COL3A1 Gene)

  • 윤유민;김동찬;강민재
    • 대한유전성대사질환학회지
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    • 제14권2호
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    • pp.168-173
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    • 2014
  • 혈관형 엘러스-단로스 증후군은 상염색체 우성 유전질환으로 COL3A1 유전자의 돌연변이로 인해 제 3형 콜라겐 합성이 결핍되면서 피부, 관절, 혈관, 폐, 내장 등에서 증상이 나타나는데 생명에 위협이 되는 합병증인 동맥 파열이나 장 천공과 같이 발생한 뒤에 진단이 늦게 내려지는 경우가 많다. 본 증례는 11세에 장천공 및 복막염의 수술력이 있는 16세 남아가 각각 운동과 경미한 손상 이후 발생한 두 차례의 근혈종으로 내원하여 시행한 COL3A1 유전자 검사에서 새로운 돌연변이 c.2931+2dupT가 발견되어 보고하는 바이다.

구강 악안면 영역의 근막간극 감염증에 관한 임상 통계학적 연구 (A CLINICOSTATISTICAL STUDY OF FASCIAL SPACE INFECTIONS OF THE ORAL AND MAXILLOFACIAL REGION)

  • 안신영;김수관;김학균;박철민
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제33권2호
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    • pp.162-168
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    • 2007
  • Oral and maxillofacial infection is the oldest and most common disease in human history. The infection ranges from the low-grade infection that only requires minimal treatment to the high-grade and life-threatening fascial space infection. In this study, the data on oral and maxillofacial infections were analyzed to aid in the diagnosis and treatment, and to predict the prognosis. This report was based on data from 831 patients with oral and maxillofacial infection (394 males and 437 females) who were hospitalized in the Department of Oral and Maxillofacial surgery of Chosun University Dental Hospital from January 1998 to May 2005. The ratio of males to females was 0.9:1. By age, patients between 60 and 70 years old were the greatest in number (17.1%), while only 5.9% of the patients were between 10 and 20 years old. The most common cause of infection was odontogenic origin (84.4%), followed by post-extraction infection (6.2%), unknown (5.9%), and trauma (3.5%). The most common fascial space involved was the buccal space (39.4%), followed by the canine (20.6%), submandibular (15.9%), pterygomandibular (9.5%), submental (7.6%) and sublingual (2.8%) space. The number of the involved fascial space was one (75.2%), two (19.8%), or more than three (5.0%). In terms of the treatment duration, the hospitalization period of 6 to 10 days was the greatest in number (49.9%). All patients had uneventful recovery without major complication. There are statistically significant correlations between age and treatment period, and the involved space and treatment period, but no correlations between the variables of sex and treatment.

Lowe 증후군 환아의 전신마취를 이용한 치료증례보고 (TREATMENT OF THE CHILD WITH LOWE SYNDROME UNDER GENERAL ANESTHESIA: A CASE REPORT)

  • 장우혁;이긍호;최영철
    • 대한소아치과학회지
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    • 제29권2호
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    • pp.237-242
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    • 2002
  • Lowe 증후군 또는 안뇌신증후군(oculocerebrorenal syndrome)은 X-염색체와 관련된 유전성 질환으로 반성열성유전양상을 나타낸다. 선천성 백내장과 녹내장 등의 안 증상, 근긴장 저하 건반사감소 등의 근신경계 증상, 신장 기능이상이 가장 특징적인 임상 증상이며, 이외에도 정신 지체, 성장지연, 전두부 융기, 가늘고 성긴 모발, 돌출된 귀, 골질환 등이 발생할 수 있다. Lowe 증후군 환자는 정신지체로 인해 치과치료시 전신마취하에서의 처치가 요구되나, 대사성 산증, 악성고열의 발생위험과 사용약제에 의한 부작용 등이 위험요소로 작용할 수 있으므로, 필요한 경우 내과 또는 소아과 의료진이 참여된 협진체제 하에서 가능한 짧은 시간 진행되어야 한다. 이러한 치과적 처치의 어려움으로 Lowe 증후군 환자에서 치과질환의 예방이 좀더 강조되어야 하면, 이를 위해 보호자의 주위의 적극적 관리가 요구된다.

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심부 경부 감염 후 합병된 흉강내 감염 2예 (Two Cases Presenting Thoracic Complications of Deep Neck Infection)

  • 염문선;김태희;김도연;정수진;이창배;이혜진;이진화;김혜영;박영식;김명래;장중현
    • Tuberculosis and Respiratory Diseases
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    • 제48권4호
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    • pp.543-549
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    • 2000
  • 저자 등은 치주 농양 및 심부 경부 감염에 합병된 급성 종격동염, 심낭 삼출, 폐렴 및 농흉 등의 흉강내 감염 2예를 경험하였으며, 위와 같은 심부 경부 감염시 흉강내 감염의 예방을 위해 조기 진단 및 완전한 배농과 적절한 항생제 등의 처치가 필요하며, 일단 흉강내 감염으로 진행시 높은 사망률을 동반할 수 있음을 문헌 고찰과 함께 보고하는 바이다.

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