nach oben

Head and Neck Pathology

Erschienen in:

19.07.2021 | Sine qua non Radiology-Pathology

Kimura Disease: A Rare and Difficult to Diagnose Entity

verfasst von: Clayton Bishop, Alyeesha Wilhelm, Duncan Watley, Felix Olobatuyi, Orly Coblens, Rohan Joshi

Erschienen in: Head and Neck Pathology | Ausgabe 1/2022

Einloggen, um Zugang zu erhalten

Abstract

Kimura disease (KD) is a rare inflammatory disorder which involves the head and neck. Due to its rarity and various findings, definitive diagnosis can be difficult to ascertain. Kimura disease is distinguished from other conditions, including angiolymphoid hyperplasia, by histopathological features including follicular hyperplasia, reactive germinal centers, abundant eosinophilia, eosinophilic microabscesses, preserved nodal architecture, Warthin-Finkeldy polykaryocytes, and capsular fibrosis. Herein, we describe the clinical presentation, pathology, and diagnosis of a single case of a 39-year-old treated at an academic center in Texas.

Othman SK, Daud KM, Othman NH. Kimura’s disease: a rare cause of nephrotic syndrome with lymphadenopathy. Malays J Med Sci MJMS. 2011;18(4):88–90.PubMed

Rascovan N, Monteil Bouchard S, Grob J-J, et al. Human polyomavirus-6 infecting lymph nodes of a patient with an angiolymphoid hyperplasia with eosinophilia or Kimura disease. Clin Infect Dis. 2016;62(11):1419–21. https://doi.org/10.1093/cid/ciw135.CrossRefPubMed

Rosai J, Gold J, Landy R. The histiocytoid hemangiomas. A unifying concept embracing several previously described entities of skin, soft tissue, large vessels, bone, and heart. Hum Pathol. 1979;10(6):707–30. https://doi.org/10.1016/S0046-8177(79)80114-8.CrossRefPubMed

Chong W-S, Thomas A, Goh C-L. Kimura’s disease and angiolymphoid hyperplasia with eosinophilia: two disease entities in the same patient. Case report and review of the literature. Int J Dermatol. 2006;45(2):139–45. https://doi.org/10.1111/j.1365-4632.2004.02361.x.CrossRefPubMed

Kempf W, Haeffner AC, Zepter K, et al. Angiolymphoid hyperplasia with eosinophilia: evidence for a T-cell lymphoproliferative origin. Hum Pathol. 2002;33(10):1023–9. https://doi.org/10.1053/hupa.2002.128247.CrossRefPubMed

Tseng C-F, Lin H-C, Huang S-C, Su C-Y. Kimura’s disease presenting as bilateral parotid masses. Eur Arch Oto-Rhino-Laryngol Head Neck. 2005;262(1):8–10. https://doi.org/10.1007/s00405-003-0677-9.CrossRef

Fouda MA, Gheith O, Refaie A, et al. Kimura disease: a case report and review of the literature with a new management protocol. Int J Nephrol. 2010;2010(2010):4. https://doi.org/10.4061/2010/673908.CrossRef

Nonaka M, Sakitani E, Yoshihara T. Anti-IgE therapy to Kimura’s disease: a pilot study. Auris Nasus Larynx. 2014;41(4):384–8. https://doi.org/10.1016/j.anl.2013.12.006.CrossRefPubMed

Kottler D, Barète S, Quéreux G, et al. Retrospective multicentric study of 25 Kimura disease patients: emphasis on therapeutics and shared features with cutaneous IgG4-related disease. Dermatology (Basel). 2015;231(4):367–77. https://doi.org/10.1159/000439346.CrossRef

10.

Hosaka N, Minato T, Yoshida S, et al. Kimura’s disease with unusual eosinophilic epithelioid granulomatous reaction: a finding possibly related to eosinophil apoptosis. Hum Pathol. 2002;33(5):561–4. https://doi.org/10.1053/hupa.2002.124037.CrossRefPubMed

11.

Lin P, Medeiros LJ. Hematopoietic lesions. In: Gnepp DR, editor. Diagnostic surgical pathology of the head and neck. 2nd ed. Philadelphia: W.B. Saunders; 2009. p. 933–74.CrossRef

12.

Chen DR, Thompson SI, Aguilera L, Abbondanzo L. Kimura disease: a clinicopathologic study of 21 cases. Am J Surg Pathol. 2004;28(4):505–13. https://doi.org/10.1097/00000478-200404000-00010.CrossRefPubMed

13.

Liu XK, Ren J, Wang XH, Li XS, Zhang HP, Zeng K. Angiolymphoid hyperplasia with eosinophilia and Kimura’s disease coexisting in the same patient: evidence for a spectrum of disease. Australas J Dermatol. 2012;53(3):e47-50. https://doi.org/10.1111/j.1440-0960.2011.00744.x.CrossRefPubMed

14.

Sia KJ, Kong CK, Tan TY, Tang IP. Kimura’s disease: diagnostic challenge and treatment modalities. Med J Malays. 2014;69(6):281–3.

Titel: Kimura Disease: A Rare and Difficult to Diagnose Entity
verfasst von: Clayton Bishop
Alyeesha Wilhelm
Duncan Watley
Felix Olobatuyi
Orly Coblens
Rohan Joshi
Publikationsdatum: 19.07.2021
Verlag: Springer US
Erschienen in: Head and Neck Pathology / Ausgabe 1/2022
Elektronische ISSN: 1936-0568
DOI: https://doi.org/10.1007/s12105-021-01359-9

Live-Webinar "Urologie und Sexualmedizin in der Praxis"

Springer Medizin

Kimura Disease: A Rare and Difficult to Diagnose Entity

Abstract

Neu im Fachgebiet Pathologie

Assistierter Suizid durch Infusion von Thiopental

Molekularpathologische Untersuchungen im Wandel der Zeit

Vergleichende Pathologie in der onkologischen Forschung

Gastrointestinale Stromatumoren

Live-Webinar "Urologie und Sexualmedizin in der Praxis"

Springer Medizin

Abstract

Bitte loggen Sie sich ein, um Zugang zu diesem Inhalt zu erhalten

Weitere Artikel der Ausgabe 1/2022

Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Familial Tumor Syndromes

Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: The Neck and Lymph Nodes, Metastasis, and Melanocytic Tumors

Orofacial Manifestations Assisting the Diagnosis of Cowden Syndrome in a Middle-Aged Patient: Case Report and Literature Overview

Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumours: Tumours of the Ear

Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Soft Tissue Tumors

Sclerosing Polycystic Adenosis Arising in the Parotid Gland Without PI3K Pathway Mutations

Neu im Fachgebiet Pathologie

Assistierter Suizid durch Infusion von Thiopental

Molekularpathologische Untersuchungen im Wandel der Zeit

Vergleichende Pathologie in der onkologischen Forschung

Gastrointestinale Stromatumoren