• 제목/요약/키워드: self-limiting disease

검색결과 53건 처리시간 0.03초

Diagnosis and Management of Ménétrier Disease in Children: A Case Series Review

  • Krikilion, Jasmina;Levy, Elvira Ingrid;Vandenplas, Yvan
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제24권1호
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    • pp.109-117
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    • 2021
  • Purpose: Ménétrier disease (MD) was first described in 1888, and 50 cases have been reported until now. We aimed to discuss the etiology, diagnostics, and management of MD in children. Methods: We searched for case reports published from 2014 till 2019 in English using PubMed. Articles were selected using subject headings and key words of interest to the topic. Interesting references of the included articles were also included. Results: The pathophysiology of MD is still uncertain. However, overexpression of transforming growth factor alpha with transformation of the gastric mucosa has been observed, which may be mediated by genetics and provoked by an infectious trigger. Clinically, MD is diagnosed by abdominal pain, vomiting, anorexia, and edema secondary to hypoalbuminemia. A gastroscopy with biopsy is the gold standard for the diagnosis of MD. In children, the disease is self-limiting and only requires supportive treatment. In general, children have a good prognosis and recover spontaneously within a few weeks. Conclusion: Few pediatric cases of MD have been described in recent years, and with all different etiology. Endoscopy with biopsy remains the golden standard for the diagnosis of MD, and in children, the disease is self-limiting.

소아에서의 아급성 괴사성 림프절염의 임상적 고찰 (Clinical Characteristics of Subacute Necrotizing Lymphadenitis in Pediatrics)

  • 김희규
    • 대한기관식도과학회지
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    • 제6권1호
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    • pp.21-28
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    • 2000
  • Background:Subacute necrotizing lymphadenitis or Kikuchi's disease is unknown ethiology and self-limiting process. This disease predominantly affects young women age but rarely affects pediatrics, and usually manifests as lymphadenopathy and fever. Even though this disease is self-limited, benign process, many cases are misidentified as malignant lymphoma. The purpose of this study is to report the clinicopathologic finding, radiological finding and many labolatory test and to compare with characteristics of adult patients in this disease. Meterial and Methods:We reviewed 27 pediarics patients with subacute necrotizing lymphadenitis by excision biopsy or fineneedle aspiration cytology.Result:The most common symptomes were palpation of cervical lymh node(88.9%) and fever(66.7%). The common site of the involvement was cervical lymph node. The multiple involvement was 93% and bilateral involvement was 59%. Leukopenia(52%) and elevated erythrocyte sedimentation rates(93%) appeared in abnormal laboratory data. Microscopically, the characteristic finding was the wide area of florid nuclear dusts engulfed by histiocytes and well-circumscrbed area with eosinophilic fibrinoid material. There was a striking degree ofkaryorrhexis and an absence of granulocyte with paucity of plasma cell. All patients recovered with the conservative treatment and there was no specific complication and recurrence. Conclusion : We reviewed pediatric patients with this disease. Characteristics of this disease inpediatric patients were similar to adult patients.

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A case of Kikuchi-Fujimoto disease with autoimmune thyroiditis

  • Go, Eun Ji;Jung, You Jin;Han, Seung Beom;Suh, Byung Kyu;Kang, Jin Han
    • Clinical and Experimental Pediatrics
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    • 제55권11호
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    • pp.445-448
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    • 2012
  • Kikuchi-Fujimoto disease (KFD) is a benign self-limiting disease characterized by fever and lymphadenitis. The etiology and pathogenesis of KFD is unclear. However, two hypotheses have been suggested: a viral infection hypothesis and an autoimmune hypothesis. Several KFD patients with various types of autoimmune diseases have been reported, and these reports support the hypothesis for autoimmune pathogenesis of KFD. Here, we report the case of a 17-year-old female patient diagnosed with KFD and autoimmune thyroiditis. This case serves as additional evidence that the etiology of KFD is autoimmune origin.

셰퍼드견에서 범골염 진단례 (Panosteitis in a German Shepherd Dog)

  • 성윤상;엄기동;이해운;이정민;장광호;오태호
    • 한국임상수의학회지
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    • 제20권2호
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    • pp.252-254
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    • 2003
  • A 18-month-old, 35.3 kg, intact male Cerman shepherd dog with a history of non-weight bearing lameness in the right hindlimb was referred to Veterinary Teaching Hospital, College of Veterinary Medicine, Kyungpook National University. On physical examination, pain response was elicited. Laboratory abnormalities were not present. Radiographic examination revealed areas of increased opacity in the medullary cavity and accentuation of trabecular patterns of the affected bone. This dog was treated with analgesics and lameness was resolved without pain.

A Case of Epiploic Appendagitis with Acute Gastroenteritis

  • Cho, Min Sun;Hwang-Bo, Seok;Choi, Ui Yoon;Kim, Hwan Soo;Hahn, Seung Hoon
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제17권4호
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    • pp.263-265
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    • 2014
  • Epiploic appendagitis is an inflammation of the epiploic appendage in which the small sacs projecting from the serosal layer of the colon are positioned longitudinally from the caecum to the rectosigmoid area. Epiploic appendagitis is rare and self-limiting; however, it can cause sudden abdominal pain in children. Epiploic appendagitis does not typically accompany other gastrointestinal diseases. Here, we report on a healthy eight-year-old girl who presented with abdominal pain, fever, vomiting, and diarrhea. Based on these symptoms, she was diagnosed with acute gastroenteritis, but epiploic appendagitis in the ascending colon was revealed in contrast computed tomography (CT). The patient was treated successfully with conservative management. CT is beneficial in diagnosis and further assessment of epiploic appendagitis. Pediatricians need to be aware of this self-limiting disease and consider it as a possible alternate diagnosis in cases of acute abdominal pain.

코로나19 공중보건 위기 상황에서의 자유권 제한에 대한 '해악의 원리'의 적용과 확장 - 2020년 3월 개정 「감염병의 예방 및 관리에 관한 법률」을 중심으로 - (Application and Expansion of the Harm Principle to the Restrictions of Liberty in the COVID-19 Public Health Crisis: Focusing on the Revised Bill of the March 2020 「Infectious Disease Control and Prevention Act」)

  • 유기훈;김도균;김옥주
    • 의료법학
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    • 제21권2호
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    • pp.105-162
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    • 2020
  • 감염병의 팬데믹 상황 속에서, 국가의 방역 대책은 안보로서의 속성을 지니며, 공중보건과 공공의 이익의 이름으로 개인의 자유에 대한 일정한 제한이 정당화되어왔다. 2020년 3월, 대한민국 국회는 「감염병의 예방 및 관리에 관한 법률」 개정안을 통과시켰으며, 이를 통해 '감염의심자'의 검사 및 격리거부에 대한 처벌의 법적 근거를 신설하고 격리위반과 치료거부의 벌칙을 상향하였다. 본 논문에서는 국가가 개인의 자유를 제한하는 행위의 정당성 판별기준에 대한 자유주의 법철학의 논변과 원리들을 검토하고, 피해자임과 동시에 매개체로서의 속성을 지니는 감염병 환자(patient as victim and vector)에 대한 자유제한원리의 적용은 파인버그(Joel Feinberg)가 제시한 '스스로에 대한 해악(harm to self)'과 '타인에 대한 해악(harm to others)'이 중첩되는 지점에 있음을 개념화하였다. 파인버그가 제기한 자유제한원리(liberty-limiting principle)를 불확실성(uncertainty)을 지니는 팬데믹 상황에 적용하기 위해서는, 해악에서 리스크(risk)로 해악의 원리를 확장시킬 것이 요구된다. 이러한 해악에서 리스크로의 전환은, 불확실한 위기상황 하에서 국가가 사전주의 원칙(precautionary principle)을 통해 개인의 자유를 사전적으로 제한하는 것을 정당화함과 동시에, 충분한 근거 없이 개인의 행위를 처벌의 대상으로 삼는 과잉범죄화(overcriminalization)의 우려를 낳는다. 본 글에서는 리스크를 지닌 개인에 대한 사전적 자유제한을 둘러싼 사전주의의 원칙과 과잉범죄화의 우려 사이에서 균형을 이룰 수 있는 원칙들을 검토한다. 이어서 '타인에 대한 해악' 원칙이 공익과 공중보건 상황에 적용되기 위한 두 번째 확장으로, 인구집단 개념으로의 전환을 다룬다. 팬데믹과 같은 공중보건 위기 상황에서는 '개인'이 아닌 '인구집단'을 하나의 단위로 고려하는 인구집단 접근법(population approach)이 필요하며, 나아가 앞선 두 논의를 결합한 '인구집단에 대한 리스크(risk to population)'가 팬데믹 상황에서 해악의 원리의 중요한 구성요소로 고려되어야 함을 제안한다. 논문의 마지막에서는, 앞서 개념화한 '확장된 해악의 원리' 하에서 개정 「감염병의 예방 및 관리에 관한 법률」의 자유제한이 정당화될 수 있는지 검토한다. 격리위반 처벌조항은 '인구집단에 대한 리스크'에 대한 자유제한에 해당하여, 강제검사 또한 무증상 감염자라는 감염병의 특성에 의거하여 '확장된 해악의 원리'의 차원에서는 정당성이 부정되지 않음을 보일 수 있었다. 그러나 치료거부 처벌조항은 전통적 해악의 원리뿐만 아니라 '인구집단에 대한 리스크'라는 팬데믹의 특성을 고려한 '확장된 해악의 원리' 하에서도 정당화되기 어려우며, 추가적 단서조항을 포함하여야만 정당화 근거를 획득할 수 있을 것임을 논증하였다.

FDG PET-CT에서 악성림프종처럼 보이는 복부 기쿠치병 (Intra-abdominal Kikuchi's Disease Mimicking Malignant Lymphoma on FDG PET-CT)

  • 한혜숙;김기현;조영심;주혜진;이옥준;류동희;이기형;김승택
    • Nuclear Medicine and Molecular Imaging
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    • 제43권4호
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    • pp.363-365
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    • 2009
  • Kikuchi's disease is a self-limiting benign disease characterized by cervical lymphadenopathy, but it can be mistaken for malignant disease, and when involved lymph nodes are unusually located, diagnosis can be more difficult. The authors report the case of a 19-year-old man with Kikuchi's disease, who had isolated intra-abdominal lymphadenopathy and increased 18-fluoro-deoxyglucose (FDG) uptake in positron emission tomography-computed tomography (PET-CT). Although its incidence is extremely rare, intra-abdominal Kikuchi's disease with increased FDG uptake in PET-CT image should be considered in the differential diagnosis when constitutional symptoms mimic those of malignant lymphoma.

Hemophagocytic lymphohistiocytosis with recurrent Kikuchi-Fujimoto disease

  • Lee, Sang Min;Lim, Young Tae;Jang, Kyung Mi;Gu, Mi Jin;Lee, Jong Ho;Lee, Jae Min
    • Journal of Yeungnam Medical Science
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    • 제38권3호
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    • pp.245-250
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    • 2021
  • Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a self-limiting lymphadenitis. It is a benign disease mainly characterized by high fever, lymph node swelling, and leukopenia. Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disease with clinical symptoms similar to those of KFD, but it requires a significantly more aggressive treatment. A 19-year-old Korean male patient was hospitalized for fever and cervical lymphadenopathy. Variable-sized lymph node enlargements with slightly necrotic lesions were detected on computed tomography. Biopsy specimen from a cervical lymph node showed necrotizing lymphadenitis with HLH. Bone marrow aspiration showed hemophagocytic histiocytosis. The clinical symptoms and the results of the laboratory test and bone marrow aspiration met the diagnostic criteria for HLH. The patient was diagnosed with macrophage activation syndrome-HLH, a secondary HLH associated with KFD. He was treated with dexamethasone (10 mg/m2/day) without immunosuppressive therapy or etoposide-based chemotherapy. The fever disappeared within a day, and other symptoms such as lymphadenopathy, ascites, and pleural effusion improved. Dexamethasone was reduced from day 2 of hospitalization and was tapered over 8 weeks. The patient was discharged on day 6 with continuation of dexamethasone. The patient had no recurrence at the 18-month follow-up.

NAG Vibrio의 검사에 관한 소고 (Study on the Identification Methods of the Non-agglutinating Vibrio)

  • 이명원
    • 환경위생공학
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    • 제2권2호
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    • pp.61-67
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    • 1987
  • The genus Vibrio contains some of the most important intestinal pathogens of humans, including Vibrio cholerae, the cause of epidemic Asiatic cholera. A group of organisms which have been reffered to as the non-agglutinating vibrio (NAG) do not agglutinate in the Vibrio cholerae 0 group 1 antisera, but are indistinguishable from the 0-1 group both chemically and genetically. Non-O-l Vibrio cholerae can cause isolated as well as focal outbreaks of diarrhea, but the volume of fluid loss does not approach that of classic cholera, and the disease is usually self-limiting. These free-living organisms are found world-widely distributed in the environment including sewage, contaminated water, estuaries, seafood and animals. These strains involved in several cases were isolated from the environment and some patients of diarrhea, and a few epidemiologic reports indicated the wide distribution of the strains throughout the country, giving an attention to the role the organisms may play in an outbreak of diarrhea in Korea. More research on the epidemiology, serologic typing and virulence of the group of organisms, should be, therefore, done to obtain a complete understanding of their role in human disease.

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소아에서 발생한 Yersinia pseudotuberculosis 감염이 동반된 아급성 괴사성 림프절염 1례 (A Case of Subacute Necrotizing Lymphadenitis Associated with Yersinia Infection in a 12 Years Old Child)

  • 심윤희;임인석;이동근
    • Pediatric Infection and Vaccine
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    • 제10권1호
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    • pp.123-126
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    • 2003
  • 저자들은 내원 10일 전부터 발현된 경부 종괴를 주소로 내원한 12세 여아에서 혈청학적 검사상 증명된 Yersinia 감염을 동반한 아급성 괴사성 림프절염 1례를 경험하였기에 이를 문헌고찰과 함께 보고하는 바이다.

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