• 제목/요약/키워드: Radiologic findings

검색결과 517건 처리시간 0.018초

Propylthiouracil 복용 후 발생한 사구체신염이 동반된 미만성 폐출혈 1예 (A Case of Diffuse Alveolar Hemorrhage with Glomerulonephritis after Propylthiouracil Treatment)

  • 이지현;김민수;이재곤;김대식;양혜진;강경우
    • Tuberculosis and Respiratory Diseases
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    • 제72권1호
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    • pp.93-97
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    • 2012
  • Propylthiouracil (PTU) is one of the most common drugs used in the treatment of Graves' disease. There are a number of side effects found with PTU use including fever, rash, arthralgia, and flu-like symptoms. Recently antineutrophil cytoplasmic antibodies (ANCA) positive vasculitis after PTU treatment was reported as a rare side effect, which can cause diffuse alveolar hemorrhage and glomerulonephritis. A 45-year-old woman with Graves' disease had been treated with PTU for five months, complained of hemoptysis due to pulmonary alveolar hemorrhage causing anemia, and also had hematuria. Simple chest X-ray and HRCT showed bilateral consolidation and bronchoalveolar lavage fluid revealed alveolar hemorrhage. A serologic test was positive for ANCA against myeloperoxidase and proteinase-3. Such findings suggested that the presence of PTU induced ANCA positive vasculitis. Cessation of PTU and the administration of high dose steroids improved the clinical manifestation, radiologic and serologic findings. We observed ANCA titer serially for 6 years. During the follow up period, ANCA titer decreased slowly and stayed within the acceptable upper normal limit.

소장의 원발성 평활근육종 2예 (Leiomyosarcoma of Small Intestine -Two cases report with literatural review-)

  • 정용식;서보양;권굉보;이태숙
    • Journal of Yeungnam Medical Science
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    • 제2권1호
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    • pp.281-286
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    • 1985
  • 소장 평활근육종은 매우 드물고 특이증상이 없으므로 원인 모를 위장관 출혈, 장폐쇄, 종물촉지, 빈혈, 복통 및 오한 등이 동반될 때 한 번은 고려하여 조기진단으로 환자의 사망율을 줄여야 할 것으로 사료된다. 최근들어 우리 나라에서도 그 증례보고가 늘어나고 본원에서도 2예를 경험한 바 이를 요약하면 1) 2예 모두 33세 남자였다 2) 발생부위는 공장 1예, 회장 1예였다 3) 주소는 1예에서는 복부통증을 동반한 종물촉지였고 다른 l 예에서는 천공에 의한 급성복막염 증상이었다. 4) 실험치상 CEA가 1예에서는 3.37에서 11.65ng/ml로 증가하였고, 다른 1예에서는 1.83 ng/ml였다. 혈색소는 술전 8.1gm%, 9.5gm%로 나타났다. Benzidine 잠혈반응은 둘 다 양성(++)였다. 5) 수술은 1예에서는 광범위 절제술 실시후 약 13개월만에 재발하여 재 수술하여 조직 검사를 다시 시행한 후 화학요법(VAC) 치료후 현재까지 외래에서 정기검진을 하고 있으며, 나머지 l예에서는 광범위 절제술후 15일만에 자진 퇴원하여 결과관철이 되지 못하고 있다.

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결핵성 공동으로 오인된 외상 후 발생한 가성 폐낭종 1예 (A Case of Post-Traumatic Pulmonary Pseudocyst Mimicking Pulmonary Cavitary Tuberculosis)

  • 이현정;강지영;임선미;지은혜;김지현;김세원;이상학;문화식;이배영
    • Tuberculosis and Respiratory Diseases
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    • 제67권5호
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    • pp.467-470
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    • 2009
  • A traumatic pulmonary pseudocyst is a rare complication of blunt thoracic trauma. The clinical symptoms and signs are similar to other respiratory diseases, such as pulmonary tuberculosis. Therefore, a trauma history with the resulting radiologic and clinical findings is important for making a diagnosis. A 26-year-old male was admitted to our hospital due to cough for 3 days. The chest x-ray revealed diffuse infiltrations and a cavitary lesion at the left lung. His left chest had hit a tree as a result of motorcycle accident one day before admission. Initially, it was assumed that his symptoms and chest X-ray might be due to a tuberculosis infection. However, bronchoscopy revealed old blood clots at both lungs, particularly in the left lower lobe bronchus. A transbronchial lung biopsy showed alveolar hemorrhage. A traumatic pulmonary pseudocyst was diagnosed from his trauma history and these findings. Computed tomography of the chest performed 4 months later showed regression of the cavitary lesion.

동맥관 개존증의 임상적 고찰 (A Clinical Study of Patent Ductus Arteriosus)

  • 조중구;박건주;김공수
    • Journal of Chest Surgery
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    • 제18권4호
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    • pp.574-581
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    • 1985
  • Surgical treatment for PDA has been pivotal in historical development of surgery for congenital heart disease. A clinical study on 36 cases of operated PDA were performed during period from Aug. 1981 to Jul. 1985 at the Department of Thoracic & Cardiovascular Surgery in Chonbuk University. The following results are obtained. 1. The 8 males and 28 females ranged in age from 2 yrs, to 24 yrs, [mean 11 yrs.] 2. Chief complaints of the patients were dyspnea on exertion in 61%, palpitation in 39%, frequent URI in 12%, and no subjective symptoms in 11%. 3. On auscultation, continuous machinery murmur heard in 94% and systolic in 14%. 4. Radiologic findings of chest P-A showed increased density of pulmonary vascularity in 94%, cardiomegaly in 69%, and within normal limits in 5% of the patients. 5. EKG findings of the patients revealed LVH in 69%, RVH in 6%, BVH in 6%, and within normal limits in 17%. 6. Of the 36 patients, cardiac catheterization was performed in 34 patients. The results showed mean Qp/Qs = 2.25, mean Pp/Ps=0.42, and mean systolic pulmonary arterial pressure=53mmHg. 7. Surgical methods were as followed: The 32 case of ductal ligation and one case of division & suture technique for PDA through the left posterolateral thoracotomy were done. And 2 cases of ductal ligation one suture closure through the pulmonary artery were performed under the cardiopulmonary bypass. 8. Intraoperative complication was ductal rupture with division 8< suture for PDA and transient hoarseness in 1, recanalization in 1, and urethral stricture in 1 case postoperatively. 9. One patient died due to ductal rupture intraoperatively and operative mortality was 2.8%.

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Korean Guidelines for Diagnosis and Management of Interstitial Lung Diseases: Part 3. Idiopathic Nonspecific Interstitial Pneumonia

  • Lee, Jongmin;Kim, Yong Hyun;Kang, Ji Young;Jegal, Yangjin;Park, So Young;Korean Interstitial Lung Diseases Study Group
    • Tuberculosis and Respiratory Diseases
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    • 제82권4호
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    • pp.277-284
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    • 2019
  • Idiopathic nonspecific interstitial pneumonia (NSIP) is one of the varieties of idiopathic interstitial pneumonias. Diagnosis of idiopathic NSIP can be done via multidisciplinary approach in which the clinical, radiologic, and pathologic findings were discussed together and exclude other causes. Clinical manifestations include subacute or chronic dyspnea and cough that last an average of 6 months, most of which occur in non-smoking, middle-aged women. The common findings in thoracic high-resolution computed tomography in NSIP are bilateral reticular opacities, traction bronchiectasis, reduced volume of the lobes, and ground-glass opacity in the lower lungs. These lesions can involve diffuse bilateral lungs or subpleural area. Unlike usual interstitial pneumonia, honeycombing is sparse or absent. Pathology shows diffuse interstitial inflammation and fibrosis which are temporally homogeneous, namely NSIP pattern. Idiopathic NSIP is usually treated with steroid only or combination with immunosuppressive agents such as azathioprine, cyclophosphamide, cyclosporine, and mycophenolate mofetil. Prognosis of idiopathic NSIP is better than idiopathic pulmonary fibrosis. Many studies have reported a 5-year survival rate of more than 70%.

Computed tomography and magnetic resonance imaging characteristics of giant cell tumors in the temporomandibular joint complex

  • Choi, Yoon Joo;Lee, Chena;Jeon, Kug Jin;Han, Sang-Sun
    • Imaging Science in Dentistry
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    • 제51권2호
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    • pp.149-154
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    • 2021
  • Purpose: This study aimed to investigate the computed tomography and magnetic resonance imaging features of giant cell tumors in the temporomandibular joint region to facilitate accurate diagnoses. Materials and Methods: From October 2007 to June 2020, 6 patients (2 men and 4 women) at Yonsei University Dental Hospital had histopathologically proven giant cell tumors in the temporomandibular joint. Their computed tomography and magnetic resonance imaging findings were reviewed retrospectively, and the cases were classified into 3 types based on the tumor center and growth pattern observed on the radiologic findings. Results: The age of the 6 patients ranged from 25 to 53 years. Trismus was found in 5 of the 6 cases. One case recurred. The mean size of the tumors, defined based on their greatest diameter, was 32 mm (range, 15-41 mm). The characteristic features of all cases were a heterogeneously-enhancing tumorous mass with a lobulated margin on computed tomographic images and internal multiplicity of signal intensity on T2-weighted magnetic resonance images. According to the site of origin, 3 tumors were bone-centered, 2 were soft tissue-centered, and 1 was peri-articular. Conclusion: Computed tomography and magnetic resonance imaging yielded a tripartite classification of giant cell tumors of the temporomandibular joint according to their location on imaging. This study could help clinicians in the differential diagnosis of giant cell tumors and assist in proper treatment planning for tumorous diseases of the temporomandibular joint.

이하선 샘암종의 재발로 오인된 지선암 1예 (A Case of Carcinoma with Sebaceous Differentiation arising in the Patient who was Treated with Parotid Gland Adenocarcinoma)

  • 박솔;윤주현;고유진;정수연
    • 대한두경부종양학회지
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    • 제38권1호
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    • pp.37-41
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    • 2022
  • Sebaceous carcinoma is extremely rare in the parotid gland. Recently, we experienced a case of carcinoma with sebaceous differentiation arising from the parotid gland in patient who was diagnosed as parotid adenoma carcinoma and underwent total parotidectomy. A 73-year-old male visited our department for the evaluation of 3-month history of infra-auricular mass combined with pain. Radiologic finding showed lobulated enhancing and solid mass with calcification in the right parotid gland. Initially, total parotidectomy with supraomohyoid neck dissection was performed. Pathological findings showed capsulated whitish mass with hemorrhage and cystic degeneration. Immunohistochemically, CK7, CK5/6, p63 were positive and CEA was negative. The intra-operative frozen section diagnosis was mucoepidermoid carcinoma. The permanent diagnosis was changed to adenocarcinoma, NOS(not otherwise specified). Fourteen months later, the newly developed mass was noticed on the operation bed. The mass was clinically diagnosed as recurred adenocarcinoma. Revision parotidectomy was performed and pathological findings revealed that the tumor was newly developed sebaceous carcinoma. We report a case of carcinoma with sebaceous differentiation in parotid gland with a review of literature.

후두에서 기원한 IgG4 연관 가성 종양 1예 (A Case of IgG4-Related Pseudotumor in Larynx)

  • 이민혁;홍준표;김태환;진성민
    • 대한후두음성언어의학회지
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    • 제33권2호
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    • pp.110-114
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    • 2022
  • IgG4-related disease is a fibroinflammatory condition by infiltration of IgG4-positive plasma cells that often presents as a tumorous lesion. This disease can affect nearly every organ system. After the pancreas, the head and neck region is second most common site for presentation of IgG4-related disease such as Mikulicz's disease, Küttner tumor. The involvement of IgG4-related disease in laryngeal lesions is extremely rare. We have experienced a case of IgG4-related disease with pseudotumor formation in the larynx that is suggestive of malignancy in radiologic findings. But the pathology findings was finally confirmed as IgG4-related disease. Oral treatment with prednisolone was initiated, and the edematous mass reduced in size without permanent functional impairment of vocal fold mobility. We report our experience with a literature review.

Clinical investigation on acute pyelonephritis without pyuria: a retrospective observational study

  • Song, Hyung Keun;Shin, Dong Hyuk;Na, Ji Ung;Han, Sang Kuk;Choi, Pil Cho;Lee, Jang Hee
    • Journal of Yeungnam Medical Science
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    • 제39권1호
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    • pp.39-45
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    • 2022
  • Background: The current guidelines for the diagnosis of acute pyelonephritis (APN) recommend that APN be diagnosed based on the clinical features and the presence of pyuria. However, we observed that some of the patients who are diagnosed with APN do not have characteristic clinical features or pyuria at the initial examination. We performed this study to investigate the characteristics of APN without pyuria. Methods: A retrospective, cross-sectional study was conducted on 391 patients diagnosed with APN based on clinical and radiologic findings, between 2015 and 2019. The clinical features, laboratory results, and computed tomography (CT) findings were compared between patients with normal white blood cell (WBC) counts and those with abnormal WBC counts (WBC of 0-5/high power field [HPF] vs. >5/HPF) in urine. Results: More than 50% of patients with APN had no typical urinary tract symptoms and one-third of them had no costovertebral angle (CVA) tenderness. Eighty-eight patients (22.5%) had normal WBC counts (0-5/HPF) on urine microscopy. There was a negative correlation between pyuria (WBC of >5/HPF) and previous antibiotic use (odds ratio, 0.249; 95% confidence interval, 0.140-0.441; p<0.001), and the probability of pyuria was reduced by 75.1% in patients who took antibiotics before visiting the emergency room. Conclusion: The diagnosis of APN should not be overlooked even if there are no typical clinical features, or urine microscopic examination is normal. If a patient has already taken antibiotics at the time of diagnosis, imaging studies such as CT should be performed more actively, regardless of the urinalysis results.

액와부 갈색지방종의 증례 보고: 초음파, 컴퓨터단층촬영, 자기공명영상, 병리 소견 (A Case Report of Axillary Hibernoma: US, CT, MR, and Histopathologic Findings)

  • 박지연;이성윤;이지영;권태정
    • 대한영상의학회지
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    • 제83권2호
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    • pp.439-443
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    • 2022
  • 갈색지방종은 갈색지방조직의 드문 양성 종양이다. 저자들은 53세 여자 환자에서 액와부 갈색지방종의 다양한 영상 소견을 보고하고자 한다. 초음파에서 오른쪽 액와부에 4.5 cm의 경계가 분명한 타원형의 비균질한 고에코의 종괴였으며, 액와부 혈관들을 앞쪽으로 전위시키고 있었다. 조영 전 흉부 단층촬영에서 5 cm의 경계가 분명한 타원형의 저감쇠의 종괴로 보였다. 자기공명영상에서는 T1과 T2 강조영상에서 비균질한 중간 및 고신호강도의 5.5 cm 종괴였으며, 변연부에서 불규칙한 조영증강을 보였다. 환자는 초음파유도중심부바늘생검을 받아 최종적으로 갈색지방종으로 진단되었다.