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Current Topics: Medical Images of Pulmonary Mycobacterioses THE CHEST CT FINDINGS AND PATHOLOGIC FINDINGS OF PULMONARY TUBERCULOSIS Hi

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Various Aspects of Acinar Lesions / H. Tokuda 557

994 _ 1000.

7 ) Hatipoglu ON, Osma E, Manisali M, et al. : High resolution computed tomographic findings in pulmonary tuberculosis. Thorax. 1996 ; 51 : 397 _ 402.

8 ) Lee JY, Lee KS, Jung KJ, et al. : Pulmonary tuberculosis : CT and pathologic correlation. J Comput Assist Tomogr. 2000 ; 24 : 691 _ 698.

9 ) 村田喜代史, 高橋雅士, 新田哲久, 他:成人肺結核症 の画像診断. 画像診断. 2000 ; 20 : 965_972.

10) 徳田 均:結核─画像診断の基礎. 診断と治療. 1999 ; 87 : 1823 _ 1829.

11) Im JG, Itoh H, Lee KS, et al. : CT-pathology correlation of pulmonary tuberculosis. Crit Rev Diagn Imaging. 1995 ; 36 : 227 _ 285. 12) 大城康二, 村山貞之, 久場睦夫, 他:肺感染症の鑑別 に役立つ CTサイン. 呼吸. 2005 ; 24 : 36_40. 13) 岡 治道:肺結核症の分類. 「戦争と結核」, 日本医事 新報社, 東京, 1943, 170_194. 14) 倉島篤行:岡ⅡB 型の胸部 X 線所見.「結核 Up to Date」 第 2 版, 四元秀毅, 倉島篤行編, 南江堂, 東京, 2005, 189 _ 190. 15) 岩崎龍郎:肺結核症の CT 画像についてのあれこれ. 資 料と展望. 1997 ; 20 : 1_27. 16) 徳田 均:慢性細葉性散布肺結核症(いわゆる岡病型 ⅡB型)の成立機序─ 2 症例からの考察. 結核. 2007 ; 82 : 507 _ 513.

17) Müller NL, Franquet T, Lee KS, et al.( 山 口 惠 三 , 石 田 直, 舘田一博訳):後天性免疫不全症候群. 「胸部画像 診断─感染症を読む」, 丸善, 東京, 2009, 138_140. 18) 倉島篤行:肺結核症と免疫. 画像診断. 2000 ; 20 : 973 _ 982. 19) 倉島篤行:ミニレクチャー 結核症の画像所見と免疫. 第 44回臨床呼吸器カンファレンス報告集. 第一三共製 薬, 東京, 2008, 37_38.

−−−−−−−− Current Topics : Medical Images of Pulmonary Mycobacterioses −−−−−−−−

VARIOUS ASPECTS OF ACINAR LESIONS

─ The Key Finding of Pulmonary Tuberculosis on HRCT─

Hitoshi TOKUDA

Abstract Acinar lesions, a pathologist’s naming for granulo-

matous lesions formed in the peripheral air space, that is, in the bronchiole or its adjacent alveolar space, is very character- istic and pathognomonic for tuberculosis on HRCT imaging. As a radiological term, it is equal to centrilobular nodule or branching shadow, or tree-in-bud appearance in the recent trend. It is universally seen in most of tuberculosis cases, irrespective of its stage or extensity. Although thus common, its appearance is not always uniform. Firstly they are not well defined in some cases. Exudative tendency in pathological process may explain for this appearance. Secondarily they are not always arranged in an orderly manner or in other words centrilobular manner on CT, but often in a random fashion. Pathologically this phenomenon can be explained by the randomness of formation site of granulomas or by scarring in spontaneous healing process of the disease. Finally, although rare, an extreme pattern, in which acinar lesions are diffusely disseminated in both lung fields without other type of lesions, is well known as Oka’s Classification of Pulmonary Tubercu-

losis Type ⅡB. This rare type of tuberculosis could be formed through indolent dissemination of bacilli via the airway or from the hematogenous dissemination. It should also be noted that in tuberculous pneumonia, especially when it develops in emphysematous lung, acinar lesions is not seen, making differential diagnosis difficult.

Key words: Acinar lesion, HRCT, Centrilobular, Tree-in-bud

appearance, Oka’s Classification of Pulmonary Tuberculosis Type ⅡB

Department of Internal Medicine, Social Insurance Central General Hospital

Correspondence to : Hitoshi Tokuda, Department of Internal Medicine, Social Insurance Central General Hospital, 3 _ 22 _ 1, Hyakunin-cho, Shinjuku-ku, Tokyo 169 _ 0073 Japan. (E-mail : tokuda@shahochu.jp)

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568 結核 第84巻 第 8 号 2009年 8 月 −−−−−−−− Current Topics : Medical Images of Pulmonary Mycobacterioses −−−−−−−−

THE CHEST CT FINDINGS AND PATHOLOGIC FINDINGS

OF PULMONARY TUBERCULOSIS

Hideo OGATA

Abstract The past research of the radiologic manifestations

of pulmonary tuberculosis in Japan was based on morpholog-ical pathology of the untreated patient autopsy. I would like to show the chest CT scan of tuberculosis diseases with caseous granuloma at its exudative reaction, proliferative reaction, productive reaction, cirrhotic reaction until self cure. This progress reflects the normal cell mediated immunological responses. Also I would like to show the cavitation of gran-uloma, which results from liquefaction of caseous materials during the course and results in the formation of the source of infection. And finally I would like to show the morphological differences of acinous lesion, acino-nodular lesion and caseous lobular pneumonia. These differences reflect the amount of bacilli disseminated in the peripheral parts under the lobules. In this study, I do not show old age cases and HIV

positive cases, who do not form typical granuloma due to the decreased cell mediated immnunity and whose X ray findings are atypical.

Key words: Pulmonary tuberculosis, Caseous granuloma,

Morphological pathology, Radiological manifestation, Chest CT scan

Respiratory Department, Fukujuji Hospital, Japan Anti-Tuber-culosis Association (JATA)

Correspondence to : Respiratory Department, Fukujuji Hospi-tal, JATA, 3_1_24, Matsuyama, Kiyose-shi Tokyo 204 _ 8522 Japan. (E-mail : ogatah@fukujuji.org)

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590 結核 第84巻 第 8 号 2009年 8 月 −−−−−−−− Current Topics : Medical Images of Pulmonary Mycobacterioses −−−−−−−−

DIFFERENTIAL DIAGNOSIS OF PULMONARY MYCOBACTERIAL INFECTION;

RADIOLOGICAL FINDINGS MIMICKING TUBERCULOUS OR

NONTUBERCULOUS MYCOBACTERIAL PNEUMONIA

1Hiroshi TANAKA, 1, 2Yuichi YAMADA, and 2Eiji ITO

Abstract Radiological imaging is one of the important clues

for diagnosis of pulmonary mycobacterial infection. Differen- tial diagnosis of pulmonary tuberculosis and nontuberculous mycobacterial infection is following ; bacterial pneumonia, bronchopneumonia, mycoplasma pneumonia, pulmonary fungal infection, diffuse panbronchiolitis, sinobronchial syn- drome, sarcoidosis, Wegener’s granulomatosis, bronchiole-alveolar carcinoma, pulmonary malignant lymphoma, and pneumoconiosis. Characteristic findings of bronchial tuber- culosis are chronic productive cough with no radiological finding, lobar atelectasis, or mucoid impaction of bronchi. Radiologic findings of pulmonary mycobacterial infection are multiple infiltration, centri-lobular nodules which sometime adhere, cavity, and solitary nodule, however, these findings mimic bacterial pneumonia and bronchopneumonia especially in case of immunosuppressive patients. Pulmonary tubercu- losis predominantly appears in upper lobe and the top of lower lobe of S6. Nontuberous mycobacterium pulmonary infection

predominantly affects middle lobe and lingual lobe, accom-panying with bronchial wall thickness and bronchiectasis. It is difficult to diagnose pulmonary mycobacterial infection using pulmonary imaging alone, therefore bacterial exami- nation from sputum or bronchoalveolar lavage fluid should be necessary.

Key words: Centri-lobular nodule, Cavity, Tuberculous

pneumonia, Differential diagnosis, Immunosuppressant

1Third Department of Internal Medicine, Sapporo Medical

University School of Medicine, 2Department of Respiratory

Medicine, Kushiro City General Hospital

Correspondence to : Hiroshi Tanaka, Third Department of In- ternal Medicine, Sapporo Medical University School of Medi- cine, South _ 1, West _ 16, Chuo-ku, Sapporo-shi, Hokkaido 060 _ 8543 Japan. (E-mail : tanakah@sapmed.ac.jp)

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Sternoclavicular Joint Tuberculosis / H. Amano et al. 595 日整会誌. 1959 ; 32 : 1071_1081. 3 ) 斉藤正史, 町田正文, 山岸正明:最近の骨・関節結核 の診断と治療. 関節外科. 2007 ; 26 : 207_214. 4 ) 川崎 剛, 佐々木結花, 篠崎 理, 他:胸鎖関節結核 の 1 例. 結核. 2007 ; 82 : 475_479. 5 ) 松田雅彦, 後藤康夫, 村 成幸, 他:結核性胸鎖関節 炎の 1 例. 肩関節. 2000 ; 24 : 271_274. 6 ) 松添大助, 安藤公英, 岩崎昭憲, 他:結核性胸鎖関節 炎を合併した粟粒結核の 1 例. 日胸. 1994 ; 53 : 723_ 726. 7 ) 川崎 拓, 松本圭司, 石澤命仁, 他:結核性胸鎖関節 炎の一例. 日関外誌. 1993 ; 12 : 311_316. 8 ) 安田 義, 田村 清, 大寺和満, 他:細菌性胸鎖関節 炎の 3 例. 整形外科. 1991 ; 42 : 239_242. 9 ) 宮本浩次, 福田真輔, 松井清明, 他:結核性胸鎖関節 炎の 1 例. 整形・災害外科. 1989 ; 32 : 1671_1674. 10) 三木信孝, 中村 勝, 加藤大輔, 他:結核性胸鎖関節 炎の 1 例. 愛媛医学. 2003 ; 22 : 86. 11) 野々村秀彦, 伊藤正志, 益田和明, 他:結核性胸鎖関 節炎の 2 例. 中部日本整形外科学会雑誌. 1994 ; 37 : 581. 12) 浅野正也, 奥江 章, 高妻雅和, 他:診断に苦慮した 結核疾患の 2 例. 整外と災外. 1984 ; 32 : 324_326. 13) De Vriese AS, Robbrecht DL, Vanholder RC, et al. : Ri-

fampicin-associated acute renal failure : Pathophysiologic, immunologic, and clinical features. Am J Kidney Dis. 1998 ; 31 : 108 _ 115.

14) 黒田文伸, 八木毅典, 山岸文雄, 他:Rifampicin の再投 与により腎障害を来した肺結核の 1 例. 結核. 1999 ; 74 : 803 _ 807.

−−−−−−−− Case Report −−−−−−−−

A CASE OF STERNOCLAVICULAR JOINT TUBERCULOSIS WITH

RENAL FAILURE DUE TO RIFAMPICIN

Hiroyuki AMANO, Mikio TAKAMORI, Akira FUJITA, Kentarou SAKASHITA, Kengo MURATA, Maki MIYAMOTO, and Akihiko WADA

Abstract A 79-year-old man was admitted to a previous

hospital complaining of left precordial swelling. Chest CT scan showed destruction of left sternoclavicular joint and a mass of 5 cm in diameter. Needle biopsy was performed and the diagnosis of sternoclavicular joint tuberculosis was made on the basis of presence of M. tuberculosis in the specimen. The patient was treated with isoniazid, ethambutol, rifampicin, and pyrazinamid but he developed renal failure. Then, he was transferred to our hospital. All medications were suspended because of the possibility of the side effect of drugs. We performed renal biopsy and histopathological examination revealed interstitial nephritis and minimal-change glomeru- lonephritis. From the result of examination, we considered interstitial nephritis was due to rifamicin. The treatment with 50 mg/day of prednisolone and isoniazid, ethambutol, and levofloxacin was administrated and renal failure and precor-

dial mass were improved. Tuberculous arthritis usually affect hip and knee joint and sternoclavicular joint involvement is very rare.

Key words: Sternoclavicular joint tuberculosis, Bone and

joint tuberculosis, Rifampicin, Drug-induced interstitial nephritis

Department of Pulmonary Medicine, Tokyo Metropolitan Fuchu Hospital

Correspondence to : Hiroyuki Amano, Department of Pulmo- nary Medicine, Tokyo Metropolitan Fuchu Hospital, 2 _ 9 _ 2, Musashidai, Fuchu-shi, Tokyo 183 _ 8524 Japan.

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Disseminated BCG Infection / S. Enkai et al. 603

−−−−−−−− Case Report −−−−−−−−

A CASE OF DISSEMINATED BCG INFECTION FOUND DURING TREATMENT OF

AN INFANT WITH CROHN’

S DISEASE

1, 5Shigehiro ENKAI, 2Tomoshi MIYAKAWA, 3Shinya KONDOU, 4Kazuteru KAWASAKI,

and 6Masaaki SEKI

Abstract Bloody stools, diarrhea and perianal abscesses

were observed from the age of two months infant. The boy received a BCG vaccination at the age of four months. The patient was diagnosed as having Crohn’s disease at the age of six months by intestinal endoscopy. Based on the diagnosis, he was treated with nutrition therapy, salazosulfapyridine, and prednisolone. Fever of unknown origin occurred two months after he had taken azathioprine at the age of two years and two months. Mycobacterium tuberculosis was detected from a gastric aspirate, and he was diagnosed as having disseminated BCG infection by means of the multiplex PCR method. Chest CT showed miliary pulmonary nodules in both lungs on admission. Physical examination revealed enlarged lymph- nodes, which were palpable around the neck and groin, and hepatomegaly. Laboratory data were within normal ranges except a slightly increased peripheral white blood cell and serum CRP level. He was treated with rifampicin (15 mg / kg / day), isoniazid (15 mg / kg / day) for 12 months, and strepto- mycin (25 mg / kg / day) for two months. He became afebrile a week after starting the treatment, and the miliary pulmonary nodules in both lungs had disappeared by 5 months after starting the treatment. An abnormality of the NEMO gene, which is the gene responsible for ectodermal dysplasia and immunodeficiency, was identified at the age of three years.

 It is assumed that an abnormality of the NEMO gene caused a latent BCG infection over a period of one year and ten months, and immunosuppressive medicine (azathioprine) induced a disseminated BCG infection. This case report supports that anti-tuberculosis medicine should be given to prevent disseminated BCG infection if an infant who receive immunosuppressive therapy is found to have an immune deficiency characterized by a mycobacterium infection after BCG vaccination.

Key words: BCG, Disseminated BCG infection, Crohn’s

disease, Abnormality of NEMO gene

1Division of General Pediatrics, and 2Division of Respiratory

Disease, Tokyo Metropolitan Kiyose Children’s Hospital,

3Department of Pediatrics, Tamahokubu Medical Center, 4Division of Respiratory Disease, National Center for Child

Health and Development, 5Department of Pediatrics, Fussa

Hospital, 6Japan BCG Laboratory

Correspondence to : Shigehiro Enkai, Department of Pediat- rics, Fussa Hospital, 1 _ 6 _ 1, Kamidaira, Fussa-shi, Tokyo 197 _ 8511 Japan. (E-mail : enkai@fussahp.jp)

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