1.Abdominal Sarcoidosis Mimicking Peritoneal Carcinomatosis.
Won Seok ROH ; Seungho LEE ; Ji Hyun PARK ; Jeonghyun KANG
Annals of Coloproctology 2018;34(2):101-105
		                        		
		                        			
		                        			We present a patient diagnosed with skin sarcoidosis, breast cancer, pulmonary tuberculosis, and peritoneal sarcoidosis with a past history of colorectal cancer. During stage work up for breast cancer, suspicious lesions on peritoneum were observed in imaging studies. Considering our patient's history and imaging findings, we initially suspected peritoneal carcinomatosis. However, the peritoneal lesion was diagnosed as sarcoidosis in laparoscopic biopsy. This case demonstrates that abdominal sarcoidosis might be considered as a differential diagnosis when there is a lesion suspected of being peritoneal carcinomatosis with nontypical clinical presentations.
		                        		
		                        		
		                        		
		                        			Biopsy
		                        			;
		                        		
		                        			Breast Neoplasms
		                        			;
		                        		
		                        			Carcinoma*
		                        			;
		                        		
		                        			Colorectal Neoplasms
		                        			;
		                        		
		                        			Diagnosis, Differential
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Peritoneum
		                        			;
		                        		
		                        			Sarcoidosis*
		                        			;
		                        		
		                        			Skin
		                        			;
		                        		
		                        			Tuberculosis, Pulmonary
		                        			
		                        		
		                        	
2.Pulmonary Sarcoidosis That Developed During the Treatment of a Patient With Crohn Disease by Using Infliximab.
Tae Kyun KIM ; Sun Hyung KANG ; Hee Seok MOON ; Jae Kyu SUNG ; Hyun Yong JEONG ; Hyuk Soo EUN
Annals of Coloproctology 2017;33(2):74-77
		                        		
		                        			
		                        			For inflammatory bowel disease (IBD), antitumor necrosis factor treatment offers a new direction for both patients and medical doctors. This treatment has dramatically improved the quality of life for patients with ulcerative colitis and Crohn disease (CD). However, with increasing usage and longer follow-up periods, a wider range of possible adverse effects may be encountered. We report an unusual case of pulmonary sarcoidosis developed during the treatment of a patient with CD by using infliximab. A 30-year-old male who had been treated for CD with infliximab for 18 months was admitted due to abnormal opacities on chest radiography. Chest computed tomography displayed clustered small nodules in both lobes and enlarged multiple lymph nodes. The patient was diagnosed with sarcoidosis from the results of a biopsy of the subcarinal lymph node. Lung lesions were improved five months after infliximab was stopped.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Biopsy
		                        			;
		                        		
		                        			Colitis, Ulcerative
		                        			;
		                        		
		                        			Crohn Disease*
		                        			;
		                        		
		                        			Follow-Up Studies
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Inflammatory Bowel Diseases
		                        			;
		                        		
		                        			Infliximab*
		                        			;
		                        		
		                        			Lung
		                        			;
		                        		
		                        			Lymph Nodes
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Necrosis
		                        			;
		                        		
		                        			Quality of Life
		                        			;
		                        		
		                        			Radiography
		                        			;
		                        		
		                        			Sarcoidosis
		                        			;
		                        		
		                        			Sarcoidosis, Pulmonary*
		                        			;
		                        		
		                        			Thorax
		                        			;
		                        		
		                        			Tumor Necrosis Factor-alpha
		                        			
		                        		
		                        	
3.Sarcoidosis Presenting with Multiple Lung Parenchymal Nodules.
Hyung Jun KIM ; Jimyung PARK ; Jee Min KIM ; Ye Jin LEE ; Hye Rin KANG ; Chang Hoon LEE
The Ewha Medical Journal 2016;39(2):61-64
		                        		
		                        			
		                        			Sarcoidosis is a multi-organ disease with various clinical manifestations. The lung is the most common site of manifestation; however, unusual findings may delay the correct diagnosis of sarcoidosis. Here we report a case of 32-year-old man with 4-month history of neck mass. Radiological findings revealed multiple pulmonary parenchymal nodules, with initial biopsy results of his neck lymph node showing chronic granuloma with focal necrosis. The patient was treated with anti-tuberculosis medications, but the size of the nodules did not change. Biopsy was performed from one of his pulmonary nodules, which revealed chronic granuloma without necrosis. Therefore, the patient was diagnosed with sarcoidosis. We present a case of sarcoidosis with multiple lung parenchymal nodules that is uncommon in Korea, with an aim to alert physicians of such unusual presentations.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Biopsy
		                        			;
		                        		
		                        			Diagnosis
		                        			;
		                        		
		                        			Granuloma
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Korea
		                        			;
		                        		
		                        			Lung*
		                        			;
		                        		
		                        			Lymph Nodes
		                        			;
		                        		
		                        			Multiple Pulmonary Nodules
		                        			;
		                        		
		                        			Neck
		                        			;
		                        		
		                        			Necrosis
		                        			;
		                        		
		                        			Sarcoidosis*
		                        			
		                        		
		                        	
4.Endobronchial Ultrasound-guided Transbronchial Needle Aspiration versus Standard Bronchoscopic Modalities for Diagnosis of Sarcoidosis: A Meta-analysis.
Li-Xing HU ; Ru-Xuan CHEN ; Hui HUANG ; Chi SHAO ; Ping WANG ; Yong-Zhe LIU ; Zuo-Jun XU
Chinese Medical Journal 2016;129(13):1607-1615
BACKGROUNDEndobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) is an effective technique used to precisely detect enlarged mediastinal lymph nodes. The efficacy of EBUS-TBNA versus standard modalities for the diagnosis of sarcoidosis remains to be elucidated. In this meta-analysis, we compared the efficacies of these methods.
METHODSWe searched PubMed, Embase, The Cochrane Library, Wanfang, Cpvip, CNKI, and the bibliographies of the relevant references. We analyzed the data obtained with Revman 5.2 (Nordic Cochrane Center, Copenhagen, Denmark) and Stata 12.0 software (Stata Corporation, College Station, TX, USA). The Mantel-Haenszel method was used to calculate the pooled odds ratio (OR) and 95% confidence intervals (CIs).
RESULTSSixteen studies with a total of 1823 participants met the inclusion criteria, and data were extracted regarding the diagnostic yield of each approach. The ORs for EBUS-TBNA versus transbronchial lung biopsy (TBLB) for the diagnosis of sarcoidosis ranged from 0.26 to 126.58, and the pooled OR was 5.89 (95% CI, 2.20-15.79, P = 0.0004). These findings indicated that EBUS-TBNA provided a much higher diagnostic yield than TBLB. The pooled OR for EBUS-TBNA + TBLB + endobronchial biopsy (EBB) versus TBNA + TBLB + EBB was 1.54 (95% CI, 0.61-3.93, P = 0.36), implying that there was no significant difference between their diagnostic yields. However, clinical heterogeneity was reflected in the nature of the studies and in the operative variables.
CONCLUSIONSThe results of this meta-analysis suggest that EBUS-TBNA + TBLB + EBB could be used for the diagnosis of sarcoidosis, if available. At medical centers without EBUS-TBNA, TBNA + TBLB + EBB could be used instead.
Biopsy, Fine-Needle ; methods ; Bronchoscopy ; methods ; Endosonography ; methods ; Female ; Humans ; Image-Guided Biopsy ; methods ; Male ; Sarcoidosis, Pulmonary ; diagnosis ; Ultrasonography ; methods
5.Granulomatous Lung Disease: A Novel Complication following Metallosis from Hip Arthroplasty.
Theodoros BALBOUZIS ; Thomas GEORGIADIS ; Peter GRIGORIS
Hip & Pelvis 2016;28(4):249-253
		                        		
		                        			
		                        			A case of a female patient with local and systemic complications of metallosis, following catastrophic wear of a revised hip arthroplasty, is presented. The patient had a history of a fractured ceramic-on-ceramic implant, exchanged with a metal-on-polyethylene prosthesis. Systemic complications included sarcoidosis-like reactions, presenting as granulomatous lung disease, along with chorioretinitis, erythema nodosum, and cardiomyopathy. High local and circulating cobalt and chromium levels established the diagnosis. The patient underwent extensive debridement and implant revision. One year postoperatively, she had no respiratory symptoms or functional impairment. Local and systemic complications of metallosis after hip arthroplasty should be promptly recognized and treated operatively.
		                        		
		                        		
		                        		
		                        			Arthroplasty*
		                        			;
		                        		
		                        			Arthroplasty, Replacement, Hip
		                        			;
		                        		
		                        			Cardiomyopathies
		                        			;
		                        		
		                        			Ceramics
		                        			;
		                        		
		                        			Chorioretinitis
		                        			;
		                        		
		                        			Chromium
		                        			;
		                        		
		                        			Cobalt
		                        			;
		                        		
		                        			Debridement
		                        			;
		                        		
		                        			Diagnosis
		                        			;
		                        		
		                        			Erythema Nodosum
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Hip*
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Lung Diseases*
		                        			;
		                        		
		                        			Lung*
		                        			;
		                        		
		                        			Prostheses and Implants
		                        			;
		                        		
		                        			Reoperation
		                        			;
		                        		
		                        			Sarcoidosis, Pulmonary
		                        			
		                        		
		                        	
6.Chitotriosidase in the Pathogenesis of Inflammation, Interstitial Lung Diseases and COPD.
Soo Jung CHO ; Michael D WEIDEN ; Chun Geun LEE
Allergy, Asthma & Immunology Research 2015;7(1):14-21
		                        		
		                        			
		                        			As a member of 18 glycosyl hydrolase (GH) family, chitotriosidase (Chitinase 1, CHIT1) is a true chitinase mainly expressed in the differentiated and polarized macrophages. CHIT1 is an innate immune mediator that digests the cell walls of chitin-containing eukaryotic pathogens, such as fungi. However, CHIT1 is dysregulated in granulomatous and fibrotic interstitial lung diseases characterized by inflammation and tissue remodeling. These include tuberclosis, sarcoidosis, idiopathic pulmonary fibrosis, scleroderma-associated interstitial lung diseases (SSc-ILD), and chronic obstructive lung diseases (COPD). CHIT1 serum concentration correlates with the progression or the severity of these diseases, suggesting a potential use of CHIT1 as a biomarker or a therapeutic target. Recent studies with genetically modified mice demonstrate that CHIT1 enhances TGF-beta1 receptor expression and signaling, suggesting a role in initiating or amplifying the response to organ injury and repair. This additional CHIT1 activity is independent of its enzymatic activity. These studies suggest that CHIT1 serves a bridging function; it is both an innate immune mediator and a regulator of tissue remodeling. This review will focus on recent data linking CHIT1 to the pathogenesis of inflammation, interstitial lung disease, and COPD.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Cell Wall
		                        			;
		                        		
		                        			Chitinase
		                        			;
		                        		
		                        			Fungi
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Idiopathic Pulmonary Fibrosis
		                        			;
		                        		
		                        			Inflammation*
		                        			;
		                        		
		                        			Lung Diseases, Interstitial*
		                        			;
		                        		
		                        			Lung Diseases, Obstructive
		                        			;
		                        		
		                        			Macrophages
		                        			;
		                        		
		                        			Mice
		                        			;
		                        		
		                        			Pulmonary Disease, Chronic Obstructive*
		                        			;
		                        		
		                        			Sarcoidosis
		                        			;
		                        		
		                        			Transforming Growth Factor beta
		                        			;
		                        		
		                        			Transforming Growth Factor beta1
		                        			
		                        		
		                        	
7.Gastric Involvement of Pulmonary Sarcoidosis.
So Hyeon HONG ; Ji Young CHANG ; Min Kyung CHUNG ; Hyo Moon SON ; Chung Hyun TAE ; Jung Hyun CHANG ; Ki Nam SHIM
The Ewha Medical Journal 2015;38(1):50-53
		                        		
		                        			
		                        			Gastric sarcoidosis is a rare disease accounting for 0.1~0.9% of all sarcoidosis cases. It presents either as a systemic disease or as an isolated finding. Diagnosis is established with biopsy of a lesion. It is important to distinguish between sarcoidosis and a sarcoid-like reaction, which can be caused by Crohn's disease, foreign body reaction, fungal infection, tuberculosis, or malignancy. We report a 60-year-old woman with both gastric and pulmonary sarcoidosis.
		                        		
		                        		
		                        		
		                        			Biopsy
		                        			;
		                        		
		                        			Crohn Disease
		                        			;
		                        		
		                        			Diagnosis
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Foreign-Body Reaction
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Rare Diseases
		                        			;
		                        		
		                        			Sarcoidosis
		                        			;
		                        		
		                        			Sarcoidosis, Pulmonary*
		                        			;
		                        		
		                        			Stomach
		                        			;
		                        		
		                        			Tuberculosis
		                        			
		                        		
		                        	
8.A Case of Papillary Thyroid Carcinoma Coexistent with Thyroid Sarcoidosis.
Nan Hee CHO ; In Wook SONG ; Sun Young KWON ; Ho Chan CHO
Journal of Korean Thyroid Association 2015;8(1):121-124
		                        		
		                        			
		                        			Sarcoidosis is a systemic granulomatous disease that primarily affects the lung and lymphatic system of the body. The involvement of thyroid gland with sarcoidosis is uncommon. Moreover, sarcoidosis with thyroid cancer are rarely reported in the world. We encountered papillary thyroid carcinoma (PTC) coexistent with pulmonary sarcoidosis. A 35-year-old female with a medical history of pulmonary sarcoidosis visited the endocrinology department for evaluation of the thyroid nodule. Thyroid ultrasonography showed multiple markedly hypoechoic nodules in the left thyroid lobe. Then ultrasonogram-guided fine needle aspiration of left thyroid nodule was positive for papillary carcinoma. She underwent total thyroidectomy with left complete cervical lymph node dissection. The histopathology was confirmed PTC combined with non-caseating granulomatous inflammation suggesting sarcoidosis on thyroid mass and lymph node. We report here a case of PTC coexistent with thyroid involvement of pulmonary sarcoidosis.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Biopsy, Fine-Needle
		                        			;
		                        		
		                        			Carcinoma, Papillary
		                        			;
		                        		
		                        			Endocrinology
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Inflammation
		                        			;
		                        		
		                        			Lung
		                        			;
		                        		
		                        			Lymph Node Excision
		                        			;
		                        		
		                        			Lymph Nodes
		                        			;
		                        		
		                        			Lymphatic System
		                        			;
		                        		
		                        			Sarcoidosis*
		                        			;
		                        		
		                        			Sarcoidosis, Pulmonary
		                        			;
		                        		
		                        			Thyroid Gland*
		                        			;
		                        		
		                        			Thyroid Neoplasms*
		                        			;
		                        		
		                        			Thyroid Nodule
		                        			;
		                        		
		                        			Thyroidectomy
		                        			;
		                        		
		                        			Ultrasonography
		                        			
		                        		
		                        	
9.Expression pattern of Mycobacterium tuberculosis Ag85B and its value in pathological diagnosis.
Nanying CHE ; Yang QU ; Chen ZHANG ; Li ZHANG ; Lijuan ZHOU ; Dan SU ; Yingli ZHAO ; Chongli WANG ; Haiqing ZHANG
Chinese Journal of Pathology 2014;43(9):600-603
OBJECTIVETo detect the expression of Mycobacterium tuberculosis secreted protein Ag85B in paraffin-embedded tissues by immunohistochemistry (IHC), and to evaluate its application in the pathological diagnosis of tuberculosis.
METHODSOne hundred and five tuberculosis specimens (54 pulmonary tuberculosis, 51 lymph nodal tuberculosis) and 51 specimens of other diseases (8 lung cancer, 10 pulmonary abscess, 10 bronchiectasis, 7 lymphoma, 5 necrotizing lymphadenitis, 4 reactive hyperplasia lymphoid, and 7 sarcoidosis) were collected from January 2012 to July 2013 from Beijing Chest Hospital, Capital Medical University. One-step IHC was performed on paraffin-embedded tissues using antibody directed against Ag85B.
RESULTSIHC and Ziehl-Neelsen (ZN) acid-fast staining showed that distribution and intensity of Ag85B expression were concordant with the distribution and number of acid-fast bacilli. IHC showed significantly higher sensitivity than ZN staining (50.5%, 53/105 vs. 31.4%, 33/105; χ² = 7.877, P = 0.005). The combined sensitivity of IHC and ZN staining was 59.0%. Moreover, oil immersion was not necessary for IHC, allowing more rapid diagnosis.
CONCLUSIONIHC detection of Ag85B is a simple method with higher sensitivity than ZN staining, and demonstrated good value in the pathological diagnosis of tuberculosis.
Acyltransferases ; metabolism ; Antigens, Bacterial ; metabolism ; Biomarkers ; metabolism ; Bronchiectasis ; diagnosis ; immunology ; Humans ; Immunohistochemistry ; Lymphadenitis ; diagnosis ; immunology ; Mycobacterium tuberculosis ; immunology ; Sarcoidosis ; diagnosis ; Staining and Labeling ; Tuberculosis, Lymph Node ; diagnosis ; immunology ; Tuberculosis, Pulmonary ; diagnosis ; immunology
10.Subcutaneous Sarcoidosis in a Patient with Myasthenia Gravis.
Sung Min PARK ; Hyun Ho CHO ; Won Jeong KIM ; Je Ho MUN ; Margaret SONG ; Hoon Soo KIM ; Byung Soo KIM ; Moon Bum KIM ; Hyun Chang KO
Korean Journal of Dermatology 2014;52(5):333-336
		                        		
		                        			
		                        			Subcutaneous sarcoidosis is rare and presents as tender or painless nodules that mostly occur on the extremities. We report a 47-year-old female patient presenting with a 1-month history of multiple asymptomatic subcutaneous nodules on the extremities. The patient had a history of myasthenia gravis for 5 years. Histopathological findings from the subcutaneous nodules showed non-caseating granulomas compatible with sarcoidosis. On inspection for internal involvement, pulmonary sarcoidosis was also detected by chest computed tomography, bronchoalveolar lavage, and transbronchial lung biopsy. The concurrence of sarcoidosis and myasthenia gravis is rare and has not been reported in the Korean literature. It may be supposed that the concurrence of these 2 separate entities is coincidental, but it has been reported that myasthenia gravis with specific antibodies is associated with sarcoidosis. This suggests that a common immunopathogenic mechanism may exist between these 2 diseases.
		                        		
		                        		
		                        		
		                        			Antibodies
		                        			;
		                        		
		                        			Biopsy
		                        			;
		                        		
		                        			Bronchoalveolar Lavage
		                        			;
		                        		
		                        			Extremities
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Granuloma
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Lung
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Myasthenia Gravis*
		                        			;
		                        		
		                        			Sarcoidosis*
		                        			;
		                        		
		                        			Sarcoidosis, Pulmonary
		                        			;
		                        		
		                        			Thorax
		                        			
		                        		
		                        	
            
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