2.Occurrence of sarcoidosis after chemotherapy for non-Hodgkin lymphoma.
Hyungwoo CHO ; Dok Hyun YOON ; Jwa Hoon KIM ; Young Bo KO ; Byoung Soo KWON ; In Hye SONG ; Cheolwon SUH
The Korean Journal of Internal Medicine 2016;31(3):605-607
No abstract available.
Drug Therapy*
;
Lymphoma, Non-Hodgkin*
;
Sarcoidosis*
3.Subcutaneous sarcoidosis presenting as a suprapubic mass, acute kidney injury, and hypercalcemia.
Jeong Min KIM ; Yoon Kyeong SONG ; Seon Jin PARK ; Young Hwan HWANG ; Su Ah SUNG ; So Young LEE ; Jong Eun JOO ; Se Won OH
The Korean Journal of Internal Medicine 2014;29(4):535-538
No abstract available.
Acute Kidney Injury/diagnosis/*etiology/therapy
;
Biopsy
;
Fluid Therapy
;
Glucocorticoids
;
Humans
;
Hypercalcemia/diagnosis/*etiology/therapy
;
Male
;
Middle Aged
;
Multimodal Imaging
;
Positron-Emission Tomography
;
Renal Dialysis
;
Sarcoidosis/*complications/diagnosis/therapy
;
Subcutaneous Tissue/pathology
;
Tomography, X-Ray Computed
;
Treatment Outcome
4.Case Report of Pulmonary Sarcoidosis Suspected to be Pulmonary Metastasis in a Patient with Breast Cancer.
Hye Sook KIM ; Suk Young LEE ; Sang Cheul OH ; Chul Won CHOI ; Jun Suk KIM ; Jae Hong SEO
Cancer Research and Treatment 2014;46(3):317-321
Standard endocrine therapy and chemotherapy can induce long-term remission in breast cancer patients; however, breast cancer can recur at any site. Pulmonary nodules with lymphadenopathy in advanced cancer patients are likely to be assumed as metastases. A 44-year-old woman with a history of breast cancer was presented to our institution with abnormal findings on 18-fluorodeoxyglucose positron emission tomography imaging, which suggested lung metastasis. She had previously been diagnosed with breast cancer (T1N2M0, Stage IIIa, intraductal carcinoma, triple negative cancer). Histological analysis of the mediastinal lymph node biopsy demonstrated sarcoidosis, showing a chronic, non-caseating, granulomatous inflammation. Our case highlights the need for non-malignant diagnoses in those with prior malignancies, and the need for histological evaluations in the event of first recurrence following potentially curative therapy.
Adult
;
Biopsy
;
Breast Neoplasms*
;
Carcinoma, Intraductal, Noninfiltrating
;
Diagnosis
;
Drug Therapy
;
Female
;
Humans
;
Inflammation
;
Lung
;
Lymph Nodes
;
Lymphatic Diseases
;
Neoplasm Metastasis*
;
Positron-Emission Tomography
;
Recurrence
;
Sarcoidosis
;
Sarcoidosis, Pulmonary*
5.Sarcoidosis Mimicking Cancer Metastasis Following Chemotherapy for Ovarian Cancer.
Mi Hyun KIM ; Kwangha LEE ; Ki Uk KIM ; Hye Kyung PARK ; Min Ki LEE ; Dong Soo SUH
Cancer Research and Treatment 2013;45(4):354-358
We report on a rare case of sarcoidosis that developed after chemotherapy for ovarian cancer, and mimicked a cancer metastasis. A 52-year-old female diagnosed with stage III ovarian cancer underwent curative surgery and postoperative chemotherapy. Four months later, her whole-body positron emission tomography and computed tomography (CT) scan showed high uptake in the mediastinal lymph nodes, and ovarian cancer recurrence was suspected. Biopsy of the mediastinal lymph nodes and subcutaneous nodules revealed noncaseating granulomas. These lesions resolved spontaneously without treatment; however, newly developed perilymphatic and centrilobular nodules were observed on follow-up chest CT. Surgical biopsy of these lesions also showed noncaseating granulomas. She was finally diagnosed with sarcoidosis.
Biopsy
;
Drug Therapy*
;
Female
;
Follow-Up Studies
;
Granuloma
;
Humans
;
Lymph Nodes
;
Middle Aged
;
Neoplasm Metastasis*
;
Ovarian Neoplasms*
;
Positron-Emission Tomography and Computed Tomography
;
Recurrence
;
Sarcoidosis*
;
Tomography, X-Ray Computed
7.Muscular Sarcoidosis Detected by F-18 FDG PET/CT in a Hypercalcemic Patient.
Eun Ji HAN ; Yi Sun JANG ; In Suk LEE ; Jong Min LEE ; Siwon KANG ; Hye Soo KIM
Journal of Korean Medical Science 2013;28(9):1399-1402
Sarcoidosis is a systemic granulomatous disease of unknown etiology that involves many organs, occasionally mimicking malignancy. We herein report a 50-yr-old woman of muscular sarcoidosis of chronic myopathic type, manifested by hypercalcemia and muscle wasting. Besides insignificant hilar lymphadenopathy, her sarcoidosis was confined to generalized atrophic muscles and therefore, F-18 FDG PET/CT alone among conventional imaging studies provided diagnostic clues for the non-parathyroid-related hypercalcemia. On follow-up PET/CT during low-dose steroid treatment, FDG uptake in the muscles disappeared whereas that in the hilar lymph nodes remained. PET/CT may be useful in the evaluation of unexpected disease extent and monitoring treatment response in suspected or known sarcoidosis patients.
Female
;
Fluorodeoxyglucose F18/*diagnostic use
;
Humans
;
Hypercalcemia/complications/*diagnosis
;
Kidney Calculi/complications/diagnosis
;
Lymph Nodes/radionuclide imaging
;
Middle Aged
;
Positron-Emission Tomography
;
Radiopharmaceuticals/*diagnostic use
;
Sarcoidosis/complications/drug therapy/*radionuclide imaging
;
Steroids/therapeutic use
;
Tomography, X-Ray Computed
8.Early-onset Childhood Sarcoidosis with Incidental Multiple Enchondromatosis.
Jong Hwa LEE ; Yeon Jung LIM ; Seunghun LEE ; Kyung Bin JOO ; Yun Young CHOI ; Chan Kum PARK ; Young Ho LEE
Journal of Korean Medical Science 2012;27(1):96-100
The triad of rash, arthritis, and uveitis seems to be characteristic for early-onset childhood sarcoidosis. We describe an interesting case of early-onset childhood sarcoidosis coexisting enchondromatosis, which clinically masquerade as Langerhans cell histiocytosis. A 33 months old girl presented with skin rash, subcutaneous nodules with polyarthritis, and revealed the involvement of lymph nodes as well as spleen during work-up. She also presented with multiple osteolytic lesions which pathologically proven enchondromatosis. Oral prednisone was prescribed at 2 mg/kg/day for 2 months until when subcutaneous nodules and joint swellings almost disappeared, and then slowly tapered over a period of 5 months. We report an unusual case of early-onset childhood sarcoidosis presented with osteolytic bone lesions which were irrelevant to sarcoidosis.
Administration, Oral
;
Anti-Inflammatory Agents/therapeutic use
;
Arthritis/complications
;
Child, Preschool
;
Diagnosis, Differential
;
Enchondromatosis/*complications/*diagnosis/drug therapy/radiography
;
Exanthema/etiology
;
Female
;
Humans
;
Positron-Emission Tomography and Computed Tomography
;
Prednisone/therapeutic use
;
Sarcoidosis/*complications/*diagnosis/drug therapy/radiography
;
Whole Body Imaging
9.Isolated Spinal Cord Neurosarcoidosis Diagnosed by Cord Biopsy and Thalidomide Trial.
Suk Won AHN ; Kyoung Tae KIM ; Young Chul YOUN ; Oh Sang KWON ; Young Baeg KIM
Journal of Korean Medical Science 2011;26(1):154-157
We report a case of 54-yr-old woman who presented with 4-extremities weakness and sensory changes, followed by cervical spinal cord lesion in magnetic resonance imaging. Based on the suspicion of spinal tumor, spinal cord biopsy was performed, and the histology revealed multinucleated giant cells, lymphocytes and aggregated histiocytes within granulomatous inflammation, consistent with non-caseating granuloma seen in sarcoidosis. The patient was treated with corticosteroid, immunosuppressant and thalidomide for years. Our case indicates that diagnosis of spinal cord sarcoidosis is challenging and may require histological examination, and high-dose corticosteroid and immunosuppressant will be a good choice in the treatment of spinal cord sarcoidosis, and the thalidomide has to be debated in the spinal cord sarcoidosis.
Adrenal Cortex Hormones/therapeutic use
;
Biopsy
;
Central Nervous System Diseases/drug therapy/pathology
;
Female
;
Humans
;
Immunosuppressive Agents/*therapeutic use
;
Magnetic Resonance Imaging
;
Middle Aged
;
Sarcoidosis/drug therapy/pathology
;
Spinal Cord/*pathology
;
Spinal Cord Diseases/drug therapy/*pathology
;
Thalidomide/*therapeutic use
10.Ocular Sarcoidosis in a Korean Population.
Sun Young LEE ; Hee Gyung LEE ; Dong Soon KIM ; June Gone KIM ; Hyewon CHUNG ; Young Hee YOON
Journal of Korean Medical Science 2009;24(3):413-419
The aim of current study was to evaluate the incidence and characteristics of ocular sarcoidosis in a Korean population. We conducted a retrospective study of 104 consecutive patients with biopsy-proven sarcoidosis seen at Asan Medical Center in Seoul, Korea, from 1993 to 2007. Medical records, photographs, and fluorescein angiograms were reviewed. Of 104 patients, 22 (21%) had intraocular involvement with female predominance (86%, M:F=3:19). Of the 39 eyes with ocular involvement, 16 (41%) eyes had isolated anterior uveitis, 12 (31%) eyes had intermediate uveitis, 6 eyes (15%) had panuveitis with retinal vasculitis, and 5 (13%) eyes had panuveitis with punched multifocal choroiditis. Mean duration of ophthalmologic follow-up was 62 months. All ocular inflammation was well managed with topical steroid and/or systemic steroid with relatively good final visual outcomes. Ocular complications such as cataract (12 eyes, 30%), glaucoma (6 eyes, 15%), vitreous opacity (1 eye, 3%), cystoid macular edema (3 eyes, 7%), neovascularization (2 eye, 5%), and epiretinal membrane (4 eye, 10%) were related to ocular sarcoidosis. In Korea, where sarcoidosis is very rare, our study indicates relatively low ocular and predominantly non posterior segment involvement with relatively good visual prognosis.
Adult
;
Age Factors
;
Asian Continental Ancestry Group
;
Choroiditis/diagnosis
;
Eye Diseases/*diagnosis/epidemiology/therapy
;
Female
;
Fluorescein Angiography
;
Humans
;
Male
;
Middle Aged
;
Retinal Vasculitis/diagnosis
;
Retrospective Studies
;
Sarcoidosis/*diagnosis/epidemiology/therapy
;
Steroids/therapeutic use
;
Uveitis, Anterior/diagnosis
;
Uveitis, Intermediate/diagnosis

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