Zobrazeno 1 - 10
of 1 120
pro vyhledávání: '"Kimura's disease"'
Publikováno v:
BMC Medical Imaging, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background ‘Kimura’s disease (KD) is a rare chronic inflammatory disorder of unknown etiology and is difficult to diagnose due to poor clinical presentation and imaging features. Few studies on characteristics of 18F-FDG PET/CT of KD hav
Externí odkaz:
https://doaj.org/article/56a10c4d85e7489590670fb25795e2da
Publikováno v:
Journal of the Korean Society of Radiology, Vol 85, Iss 5, Pp 943-947 (2024)
Kimura’s disease (KD) is a rare, chronic inflammatory disorder characterized by angiolymphoid hyperplasia, peripheral eosinophilia, and elevated serum immunoglobulin E levels. It primarily affects young Asian males and typically involves the head
Externí odkaz:
https://doaj.org/article/8f6dd3e2132940598213bb1826551e0c
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 25, Iss 3, Pp 237-239 (2024)
Cutis marmorata telangiectatica congenita (CMTC) is a rare capillary malformation characterized by persistent reticulated marbled erythema. A 16-year-old boy presented with reddish net-like lesion over the left side of his body which was initially no
Externí odkaz:
https://doaj.org/article/0dfaeb6c5c364a2cb0240882d5167ea9
Autor:
Pavithra Sarda, Prashanthi Gurram, Karthik Ramakrishnan, Vivek Narayanan, Saravanan Chandran, Divya Vinayachandran
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-9 (2024)
Abstract Background Head and neck are a site of numerous pathologies with different aetiologies and presentations. Rare pathologies, although infrequent still do exist. Diagnostic dilemma in maxillofacial pathologies can be the most challenging situa
Externí odkaz:
https://doaj.org/article/81396a21eaa84451a7c7f96125112d50
Autor:
Zablon Mesfin Anbessie
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-4 (2024)
Abstract Background Kimura’s disease is a rare chronic inflammatory disorder of unknown etiology that is seen in people of Asian descent. It is characterized by head and neck subcutaneous nodules along with lymphadenopathy, which is usually solitar
Externí odkaz:
https://doaj.org/article/4787567ef11542a08bc3f0b75e6214e3
Autor:
Géssica Sabrine Braga Barbosa, Precil Diego Miranda de Menezes Neves, Sara Mohrbacher, André Néder Ramires Abdo, Lívia Barreira Cavalcante, Yara de Menezes, Victor Augusto Hamamoto Sato, Érico de Souza Oliveira, Leonardo Victor Barbosa Pereira, Alessandra Martins Bales, Marcella Martins Frediani, Pedro Renato Chocair, Américo Lourenço Cuvello-Neto
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionKimura’s disease (KD) is a rare chronic inflammatory disorder characterized by subcutaneous lymphoid hyperplasia with peripheral eosinophilia. Kidney involvement is reported in 15%–18% of adult patients with KD, in many cases as nephr
Externí odkaz:
https://doaj.org/article/3f7628a3d5334e4aa53edb878ab149fd
Akademický článek
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Autor:
Baodi Yang, Hailan Liao, Minghua Wang, Qiaoyan Long, Huanhuan Zhong, Lin Luo, Zhongmin Liu, Xiaohui Cheng
Publikováno v:
BMC Ophthalmology, Vol 22, Iss 1, Pp 1-10 (2022)
Abstract Background Kimura’s disease is a rare, benign, chronic inflammatory disease that presents as painless, solid masses mainly affecting the deep subcutaneous areas of the head and neck, especially the salivary glands, parotid glands and nearb
Externí odkaz:
https://doaj.org/article/b48f3d179a3a4e95b0669925dec380df
Autor:
Pooja Medikonda, Satya Tejaswi Akula, Ravikanth Manyam, P Swetha, Kishore Moturi, Ramesh Tatapudi
Publikováno v:
Journal of Dr. NTR University of Health Sciences, Vol 11, Iss 3, Pp 246-250 (2022)
Angiolymphoid hyperplasia with tissue eosinophilia (ALHE) is a rarely occurring benign vascular tumor of unknown etiology and most commonly affecting the head and neck region. It usually presents clinically as brownish or purplish papules or nodules
Externí odkaz:
https://doaj.org/article/ad00ee3b442d4870aa552202accd355e
Autor:
Qing Han, Jie Han, Weitao Wang, Jie Gao, Youzhen Qiao, Junfeng Jia, Kui Zhang, Zhaohui Zheng, Ping Zhu
Publikováno v:
Frontiers in Medicine, Vol 9 (2023)
Kimura's disease (KD) is a rare chronic progressive immune inflammatory disease. The etiology is unknown and manifests as a chronic inflammatory process, which is more common in young Asian men. The clinical manifestations are painless subcutaneous s
Externí odkaz:
https://doaj.org/article/c5a66875ce1e4d988f9aaa7f94fd991b