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Brief Case Report
- Necrotizing Sarcoid Granulomatosis: Possibly Veiled Disease in Endemic Area of Mycobacterial Infection
- Yosep Chong, Eun Jung Lee, Chang Suk Kang, Tae-Jung Kim, Jung Sup Song, Hyosup Shim
- J Pathol Transl Med. 2015;49(4):346-350. Published online June 1, 2015
- DOI: https://doi.org/10.4132/jptm.2015.04.17
- 7,423 View
- 74 Download
- 11 Web of Science
- 11 Crossref
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Citations
Citations to this article as recorded by
- Sarcoidosis With Skeletal Involvement Masquerading as Metastatic Malignancy
Arthur M Samia, Stephanie Fabara Pino, Liang Sun
Cureus.2023;[Epub] CrossRef - Necrotic sarcoid granulomatosis – a late stage of nodular sarcoidosis or an independent disease? Analysis of a clinical case
E. A. Galushko, E. V. Pozhidaev, S. G. Radenska-Lopovok, A. V. Gordeev, M. V. Shaligina, A. V. Alekseeva, M. A. Sedelnikova
Rheumatology Science and Practice.2023; 61(5): 624. CrossRef - Incidental Lung Cavity in the Heartland
Biplab K. Saha, Om Dawani, Woon H Chong, Alyssa Bonnier
The American Journal of the Medical Sciences.2022; 363(2): 191. CrossRef - A rare presentation of necrotizing sarcoidosis
Nirali Sheth, Umaima Dhamrah, Branden Ireifej, David Song, Penpa Bhuti, Jagbir Singh, Henry Fan, Sibghatallah Ummar, Vikash Jaiswal, Nishan Babu Pokhrel
Respirology Case Reports.2022;[Epub] CrossRef - Necrotizing Granulomatous Dacryoadenitis With Non-Necrotizing Granulomatous Scar Hypertrophy: Two Histological Variants of Sarcoidosis in the Same Patient
Erin E. Godbout, M. Kristina Subik, Tal J. Rubinstein
Ophthalmic Plastic & Reconstructive Surgery.2021; 37(1): e30. CrossRef - Necrotizing sarcoid granulomatosis simulating pulmonary malignancy
Jun Hyeok Kim, Bo Da Nam, Jung Hwa Hwang, Dong Won Kim, Ki-Up Kim, Young Woo Park
Medicine.2021; 100(49): e28208. CrossRef - Necrotizing Sarcoid Granulomatosis: A Disease Not to be Forgotten
A. I. Parejo-Morón, M. L. Tornero-Divieso, M. R. Férnandez-Díaz, L. Muñoz-Medina, O. Preda, N. Ortego-Centeno
Case Reports in Medicine.2020; 2020: 1. CrossRef - Clinical Reasoning: A woman with monocular vision loss
Husain Danish, Tatiana Bakaeva, Isaac Solomon, Sashank Prasad
Neurology.2020;[Epub] CrossRef - Cavity forms of thoracic sarcoidosis (literature review, clinical and radiological observations)
A. V. Lenshin, A. V. Il'in, Yu. M. Perelman
PULMONOLOGIYA.2020; 30(6): 831. CrossRef - Thoracic sarcoidosis versus tuberculosis: Need for a multi-disciplinary approach
Agrima Mian, Animesh Ray
Indian Journal of Radiology and Imaging.2018; 28(02): 267. CrossRef - Necrotizing sarcoid granulomatosis with clinical presentations of recurrent acute abdomen. Case report and literature review
V. I. Vasilyev, S. G. Palshina, B. D. Chaltsev, S. G. Radenska-Lopovok, T. N. Safonova
Terapevticheskii arkhiv.2017; 89(11): 60. CrossRef
- Sarcoidosis With Skeletal Involvement Masquerading as Metastatic Malignancy
Case Reports
- Pseudofungi Associated with a Granulomatous Response in a Lymph Node: A Case Report.
- Haeryoung Kim, Ja Seung Koo, Hyosup Shim, Gijong Yi, Sang Ho Cho
- Korean J Pathol. 2004;38(1):64-67.
- 1,559 View
- 13 Download
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Abstract
PDF - . We present herein a case of pseudofungi incidentally found in the mediastinal lymph nodes of a 31-year-old woman who had a left pneumonectomy for a pulmonary blastoma. The pseudofungi were located in the subcapsular sinuses of the lymph nodes with an associated granulomatous reaction. They revealed yellowish-brown hyphae-like structures with pseudosepta and irregular branching at various angles intermingled with round yeast-like forms. These structures stained positively with periodic acid-Schiff and Gomori methenamine silver, but also stained strongly positive for Prussian blue suggesting that they contain iron. The characteristic morphological features of pseudofungi are discussed with emphasis on the features that distinguish them from true fungal organisms.
- Alagille Syndrome: A Case Report.
- Hyosup Shim, Chanil Park, Soon Il Kim, Young Nyun Park
- Korean J Pathol. 2004;38(1):56-59.
- 2,522 View
- 80 Download
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Abstract
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- Alagille syndrome is a rare autosomal dominant disorder showing complicated systemic manifestations, although the hepatic manifestations are predominant in many patients. We report a case of Alagille syndrome in a male baby who presented with a heart murmur at 2 days old and his echocardiography showed aortic stenosis. He presented with acholic stool and jaundice at 3 months old and a liver biopsy revealed paucity of the interlobular bile duct in the portal tract. This progressed to cirrhosis, for which a liver transplantation was performed at 10 months old. The explanted liver showed biliary-type cirrhosis with severe cholestasis. There was an absence of the interlobular bile ducts on microscopic examination. Bile duct paucity, associated with cholestasis, a peculiar face (prominent forehead, deep-set eyes, pointed mandible and bulbous nasal tip), and cardiac anomaly were observed, which were consistent with Alagille syndrome. He died of heart failure.
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