• 제목/요약/키워드: Granuloma

검색결과 437건 처리시간 0.033초

A Lung Granuloma Case Possibly Associated with a Working Environment: A Case Report

  • Seehapanya, Sankom;Chaiear, Naesinee;Ratanawatkul, Pailin;Samerpitak, Kittipan;Intarawichian, Piyapharom;Wonglakorn, Lumyai
    • Safety and Health at Work
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    • 제12권2호
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    • pp.268-271
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    • 2021
  • Lung granulomas are uncommon in Thailand. The disease typically develops from an occupational environment and is mostly caused by infection. Herein is a case report of a female patient, aged 48, working as a nurse in an Accident and Emergency Department at a hospital. Eighteen years prior to admission the patient was diagnosed with myasthenia gravis and pulmonary tuberculosis. The chest X-ray and CT scans showed a solitary pulmonary nodule in the lower left lung. The patient received an open thoracotomy with a left lobectomy. Granulomatous and nonseptate hyphae were found in the pathology diagnosis. The patient was thus diagnosed as having a lung granuloma. The galactomannan antigen test was positive. The solitary pulmonary nodule-found from the use of a Polymerase Chain Reaction (PCR) test-was an Aspergillus spp. The fungus culture was collected from air samples. The air samples were collected by the impaction technique using a microbial air sampler. Three types of Aspergillus spp. were found as well as Penicillium spp. and Monilia sitophila. The Aspergillus spp. was a match for the patient's disease. The patient was diagnosed as having a lung granuloma possibly Aspergillus nodule which was caused by airborne Aspergillus spp. from the occupational environment.

후두 종양의 임상적 및 병리조직학적 고찰 (The Clinical and Histopathological Study of Laryngeal mass)

  • 김화성;한경수;이준기;정덕희;박재훈
    • 대한기관식도과학회:학술대회논문집
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    • 대한기관식도과학회 1981년도 제15차 학술대회연제순서 및 초록
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    • pp.9.1-10
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    • 1981
  • 1975년 3月부터 1980년 3月까지 애성을 주소로 하여 본원에 입원하여 수술 받은 183명의 후두 종양 환자에 대한 임상적 통계와, 그중 병리조직학적으로 확진된 88case의 성대 결절과 폴립 환자에서, 성대 결절(30case), 국한성 폴립 (48), 미만성 폴립 (10)을, 임상적인 분류하에 현미경학적 검사로 다음과 같은 결과를 얻었기에 보고하는 바이다. I. 임상적 관찰 1) 전체 183명중 성대 결절 82명 (45%), 후두 폴립 53명 (29%), 삽관후 육아종 3명 (1%), 후두 유두종 18명 (10%), 후두 결핵 2명 (1%), 후두암 25명 (14%)를 차지했다. 2) 남녀 비는 성대 결절 3 : 4, 후두 폴립은 1 : 1, 삽관후 육아종 1 : 2, 후두 유두종 3 : 2, 후두암 11 : 1.성대 결절, 삽관후 육아종은 여자, 후두암과 후두 유두종은 남자에게 많았다. 3) 연령 분포는 성대 결절 20~30대, 후두 폴립 30~40대, 삽관후 육아종 20대, 후두 결핵 10대와 40대, 후두암은 50대이었다. 4) 증상발현으로부터 내원까지의 이환기간의 분포를 보면 성대 결절과 폴립은 5개월~1년, 후두 유두종과 삽관후 육아종은 1년이내, 후두 결핵과 암은 1년~3년이었다. 5) 발생 부위를 보면, 성대 결절, 폴립 후두 유두종은 성대의 전 1/3~중 1/3경계, 삽관후 육아종은 중 1/3~후 1/3, 이었다. 6) 발생측에 있어서 후두 결절과 유두종은 성대의 양측에 오며, 후두 폴립 5 : 3, 삽관후 육아종 2 : 1로 우측에 많았다. 7) 후두 종양의 크기는, 성대 결절 1~2mm(67%), 후두 폴립 3~5mm(42%), 삽관후 육아종 6~10mm(67%), 후두 유두종 1~2mm(39%), 후두 결핵과 암은 10mm 이상의 크기로 산재해 있었다. 8) 후두 종양의 증상은 애성이 90%이상, 연하통은 후두암과 결핵, 호흡곤란은 삽관후 육아종, 후두 유두종, 결핵, 암에서 나타났으며, 그외에 후두의 이물감, 작열감, 소양감 둥의 증상이 있었다. 9) 과거력은 Smoking과 관련 있는 것이 후두 결핵 50%, 후두암 40%이었고, 후두 유두종은 빈번한 상기도 감염이 33%에서 있었다. 10) 직업에서는 어떤 특별한 통계학적 의미를 찾아볼 수 없었다. II. 병리조직학적 관찰 1) 성대 결절과 플립의 상피세포는 중층 편평 상피로 덮여 있으나, 위축, 극세포증, 이상 각화증과 과각화증의 소견을 보이며, 그중 과각화증과 극세포증이 많았다. 2) WHO classification에 의해 섬유성 점액 종양, 혈관성, 유리질성의 4가지 단계로 나누였는데, 성대결절은 점액 종양 병변 60%, 국한성 폴립은 점액 종양 병변과 함께 혈관성, 유리질성 병변이 많았고, 미만성 폴립은 혈관성 병변(80%)이었다. 3) 전 18례의 후두 유두종에서, Exophytic 형이며 편평세포형이 17례(94.5%), 역형이며 이행세포형이 1례 (5.5%)이었다. 4) 후두암은 편평세포 : 선암의 비율이 24 : 1이었다.

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A Protective Mechanism in Lungs of Rats Experimentally Infected with Aspergillus fumigatus

  • Mahmoud, Yehia A.G.;Al-Ghamdi, Abdulaziz Yahya;Abd El-Zaher, Eman H.F.
    • Mycobiology
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    • 제39권1호
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    • pp.40-44
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    • 2011
  • Aspergillus fumigatus is associated with invasive disease aspergillosis in immunocompromised individuals. The major aim of this study was to investigate the biochemical and immunological responses of male Wistar rats against A. fumigatus experimentally-induced pulmonary fungal infection. Nostril experimental exposure of male Wistar rats to a high dose of A. fumigatus freeze-dried preparation for only 24 hr resulted in a significant increase in levels of catalase, nitric oxide and lipid peroxide in lung homogenates, compared to those of the control animals. However, the oxidative status of the lungs of rats challenged with killed fungus did not change significantly, except for the stimulation in the level of lipid peroxide. IgG level was significantly elevated only in rats that received two low doses of fungus, compared to unexposed animals (p < 0.005). Examining the lung of rats exposed to A. fumigatus revealed no abnormal changes, except for pus in bronchial lumen spaces and per bronchial inflammation. Histologically, large numbers of granuloma cells were evident in the lungs of challenged rats, while no granuloma formation was evident in the lungs of rats exposed to killed fungus.

전두부에 발생한 랑게르한스세포 조직구증의 치험례 (A Case Report of Langerhans Cell Histiocytosis of Frontal Area)

  • 양해원;강민구;장충현
    • 대한두개안면성형외과학회지
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    • 제10권1호
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    • pp.37-39
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    • 2009
  • Purpose: Langerhans cell histiocytosis is a heterogenous group of Langerhans cell proliferative disorders and includes eosinophilic granuloma, Letterer-Siwe diseases, and Hand-Schuller Christian disease. We report a case of eosinophilic granuloma on frontal area. Methods: A 17-year-old male presented with swelling and tenderness on Lt. frontal and periorbital area. CT and MRI showed a $33{\times}25mm$ sized mass that involved Lt. frontal calvarium, frontotemporal meninges, and orbital roof. Results: Total excision of the mass and adjacent soft tissue, calvarium, and orbital roof was performed. Orbital roof defect was reconstructed with absorbable plate and calvarial defect was done with outer cortex of temporal bone flap. The histology revealed proliferation of histiocytes and eosinophils. Immunologically, these histiocytic cells expressed S-100 protein and CD1a. The patient is currently taking conservative treatment. Conclusion: The severity of these disease and their prognosis and treatments are various. For unifocal cranial Langerhans cell histiocytosis, complete excision is the treatment of choice. We report this case with review of literature.

조직구 증식증 X (HISTIOCYTOSIS X)

  • 전혜경;오성섭;김일규;노상엽
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제18권4호
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    • pp.718-725
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    • 1996
  • Histiocytosis X is the abnormal proliferation of histiocytes and usually a massive aggregation of eosinophilic leukocytes. The clinical features and prognosises of subclasses of histiocytosis X depend on the severity and extent of the organ involvement. The subclasses include Letterer-Siwe disease(Acute disseminated histiocytosis X), eosinophilic granuloma, Hand-Schuller-Christian disease. Letterer-Siwe disease(acute, subacute form) refers to the form of disease that is most often fatal because of the widespread skeletal, extraskeletal lesion ; this usually affects infants and children less than 3 years of age. Eosinophilic granuloma(histiocytosis X, localized) refers to a chronic form of disease with skeletal lesion ; It usually affects children and young adult. Hand-Schuller-Christian disease(chronic form) refers to a chronic form of disease with skeletal, extraskeletal lesions. It usually affects children over the age of 3 years. In our hospital, 8 year old female patient visited complaining of hard swelling of mandibule body, left side and 6 year old female patient visited complaining of painful swelling of mandibular angle, right side. We diagnosed eosinophilic granuloma and curetted the lesiones and refered to Dept. pediatrics for chemotherapy. We present 2 cases to you with literatures.

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이물 육아종으로 오인된 심부 열상 이후 발생한 비정상적인 내측 족저 신경의 외상성 신경종: 증례 보고 (Unusual Presentation of Traumatic Neuroma of the Medial Plantar Nerve after Deep Laceration Mimicking a Foreign Body Granuloma: A Case Report)

  • 우승훈;김태우;배정연
    • 대한족부족관절학회지
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    • 제21권4호
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    • pp.174-178
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    • 2017
  • Traumatic neuromas are rare benign tumors that are common after trauma or surgery and are usually accompanied by obvious symptoms of pain. Most reports show neuromas in the face, neck, and limbs, and the traumatic neuroma of the medial plantar nerve has rarely been reported. We encountered a traumatic neuroma of the medial plantar nerve after a deep laceration mimicking a foreign body granuloma. A small mass lesion was found around plantar aponeurosis with heterogeneous high signal intensity in the T2 fat suppression view and slightly enhanced intensity in the magnetic resonance imaging that suggested a foreign body granuloma. The lesion was diagnosed pathologically as a traumatic neuroma. A satisfactory clinical result was obtained after excision of the traumatic neuroma and burial of the proximal and distal stumps to the adjacent muscle at the secondary operation.

중앙성육아종의 방사선치료 (Radiation Therapy (RT) of Midline Granuloma)

  • 권형철;오윤경;길학준;윤세철;박용휘
    • Radiation Oncology Journal
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    • 제4권2호
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    • pp.135-139
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    • 1986
  • 중앙성육아종 환자 7예에 대하여 가톨릭의대 강남성모병원 방사선치료실에서는 1983년 3월 부터 1986년 6월까지, 사이에 외부방사선치료를 시행하였다. 임상증상으로서, 모든 환자에서 침습부위에 궤사를 동반한 부비동염 증세를 보였고, 1예에선 대장(결장)병변도 나타냈다. 방사선치료는 6MV선형가속기를 사용하여 비강 및 부비동 부위를 포함하는 상기도 부위에 $2\~3$문 조사를 실시하여, 총선량 $4,000\~5,000cGy/5\~6$주를 조사하였다. 방사선치료 반응으로서 방사선치료 종료 후 $1.5\~20$개월 추적관찰 한 결과 완전 및 부분관해가 각각 3예, 대장부위에 병변을 보였던 1예에선 병이 진행되고 있음이 관찰되었다.

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Cutaneous Sterile Pyogranuloma/Granuloma Syndrome in an Old English Bulldog: Case Report

  • Yoon, Ji-Seon;Bae, Hyeona;Ahn, Soomin;Hong, Il-Hwa;Jung, Dong-In;Park, Jinho;Yu, DoHyeon
    • 한국임상수의학회지
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    • 제36권6호
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    • pp.345-348
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    • 2019
  • A four-year old, indoor-living neutered male Old English Bulldog was presented for generalized ulcerative dermatitis. Generalized alopecia and multifocal papules and ulcers with crusting were observed mainly in the dorsal trunk. Cytology of the skin lesions revealed a pyogranulomatous inflammation comprising macrophages and nondegenerate neutrophils. Histopathology also revealed a nodular dermatitis characterized by mixed infiltration of monocytes and neutrophils involving the superficial and deep dermis. Neither of bacteria nor fungus was identified in microscopic exam and culture. From those findings, a diagnosis of cutaneous sterile pyogranuloma/granuloma syndrome (SPGS) was made. Treatment with immunosuppressive drugs of prednisone and cyclosporine was performed and visible ulcerative skin lesions were resolved after 4 weeks of initiation of therapy. Treatment with combination of cyclosporine and prednisone may be effective for the case of SPGS.

Cone-beam computed tomographic imaging of central giant cell granuloma: A comprehensive review

  • Tahmasbi-Arashlow, Mehrnaz;Patel, Paras B.;Nair, Madhu K.;Liang, Hui;Cheng, Yi-Shing Lisa
    • Imaging Science in Dentistry
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    • 제52권2호
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    • pp.123-131
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    • 2022
  • Purpose: The aim of this study was to characterize the cone-beam computed tomographic (CBCT) imaging features of central giant cell granuloma (CGCG) of the jawbone. Materials and Methods: This study retrospectively reviewed 26 CBCT studies of histologically proven cases of CGCG during a period of 20 years, from 1999 to 2019. Patients' demographic data were recorded, and radiographic features were assessed (location, border, cortication, appearance of the internal structure, locularity, septation, expansion, cortical perforation, effects on surrounding tissue, whether the lesion crossed the midline, and lesion volume). Results: In this study, CGCGs were seen almost twice as often in the mandible than in the maxilla, and 64.7% of mandibular lesions involved the anterior region. Only 26.9% of lesions crossed the midline, a feature that was considered characteristic of CGCG. Furthermore, 65.4% of lesions were unilocular and 34.6% were multilocular. The correlation between a lesion's size and its locularity was statistically significant, and larger lesions showed a multilocular appearance. The mean volume of multilocular lesions was greater than that of unilocular lesions. Conclusion: CGCGs showed variable radiographic features on CBCT, and this imaging modality is highly effective at demonstrating the radiographic spectrum and lesional extent of CGCGs in the jawbone.

Eosinophilic Granuloma Treated with Prednisolone and Azathioprine in a Dog

  • Jang, Moonseok;Lee, Wanghui;Park, Seongjun
    • 한국임상수의학회지
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    • 제39권4호
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    • pp.192-196
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    • 2022
  • A two-year-old, intact male, 45 kg Doberman Pinscher was referred with dermal nodular lesions affecting the left hindlimb. The cytological examination revealed eosinophilic inflammation. Skin biopsy specimens showed canine eosinophilic granuloma (CEG). The dog was administered oral prednisolone (1.5 mg/kg/day) and azathioprine (2 mg/kg/day). After one week, the skin lesions diminished dramatically, but the dog presented with severe watery diarrhea. The prednisolone dose was reduced by 0.9 mg/kg/day. The lesions and diarrhea improved markedly after one week. Prednisolone was tapered by 25% of the previous dose every week to 0.2 mg/kg/day. Azathioprine was also reduced to therapy every other day. After seven weeks of combination treatment, the medications were withdrawn, but the dog had a recurrence one week later. Azathioprine (2 mg/kg/EOD) was reintroduced for two weeks. There was no relapse after all the medications had been withdrawn. This case indicates that CEG can be managed with prednisolone and azathioprine. Azathioprine may be an effective adjunctive immunosuppressive agent, and may be considered as a well-tolerated prednisolone sparing agent to treat CEG.