Difference between revisions of "Kimura disease"

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'''Kimura disease''' is a rare disease with abundant eosinophils.  It may show-up in a [[lymph node]] specimen.
{{ Infobox diagnosis
| Name      = {{PAGENAME}}
| Image      = Kimura_disease_-_very_high_mag.jpg
| Width      =
| Caption    = Kimura disease. [[H&E stain]].
| Micro      = eosinophils and thick walled [[blood vessel]]s with [[hobnail]]ed endothelial cells
| Subtypes  =
| LMDDx      = [[angiolymphoid hyperplasia with eosinophilia]], [[drug reaction]], infection (parasitic), [[lymphoma]], [[LCH]]
| Stains    =
| IHC        =
| EM        =
| Molecular  =
| IF        =
| Gross      =
| Grossing  =
| Site      = [[lymph node]], head and neck
| Assdx      =
| Syndromes  =
| Clinicalhx =
| Signs      =
| Symptoms  =
| Prevalence = extremely rare
| Bloodwork  = eosinophilia
| Rads      =
| Endoscopy  =
| Prognosis  =
| Other      =
| ClinDDx    =
}}
'''Kimura disease''' is a rare disease with abundant eosinophils.  It may show-up in a [[lymph node]] specimen. It is similar to ''[[angiolymphoid hyperplasia with eosinophilia]]''.<ref>URL: [http://emedicine.medscape.com/article/1082603-overview http://emedicine.medscape.com/article/1082603-overview]. Accessed on: 14 January 2012.</ref>


==General==
==General==
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Features:<ref name=Ref_ILNP190>{{Ref ILNP|190}}</ref>
Features:<ref name=Ref_ILNP190>{{Ref ILNP|190}}</ref>
*Angiolymphoid proliferation.
*Angiolymphoid proliferation.
**Thick walled blood vessels with (plump) hobnail endothelial cells.<ref>URL: [http://emedicine.medscape.com/article/1098777-diagnosis http://emedicine.medscape.com/article/1098777-diagnosis]. Accessed on: 8 August 2010.</ref>
**Thick walled blood vessels with (plump) [[hobnail]] endothelial cells.<ref>URL: [http://emedicine.medscape.com/article/1098777-diagnosis http://emedicine.medscape.com/article/1098777-diagnosis]. Accessed on: 8 August 2010.</ref>
*Eosinophils - abundant - '''key feature'''.
*Eosinophils - abundant - '''key feature'''.


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*Drug reaction.
*Drug reaction.
*Parasitic infection.
*Parasitic infection.
*[[Angiolymphoid hyperplasia with eosinophilia]].


Notes:
Notes:
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*Abundant eosinophils: consider [[Langerhans cell histiocytosis]].
*Abundant eosinophils: consider [[Langerhans cell histiocytosis]].


Images:
===Images===
*[http://commons.wikimedia.org/wiki/File:Kimura_disease_-_very_high_mag.jpg Kimura disease - very high mag. (WC)].
<gallery>
*[http://commons.wikimedia.org/wiki/File:Kimura_disease_-_high_mag.jpg Kimura disease - high mag. (WC)].
Image:Kimura_disease_-_very_high_mag.jpg | Kimura disease - very high mag. (WC)
*[http://commons.wikimedia.org/wiki/File:Kimura_disease_-_intermed_mag.jpg Kimura disease - intermed. mag. (WC)].
Image:Kimura_disease_-_high_mag.jpg | Kimura disease - high mag. (WC)
Image:Kimura_disease_-_intermed_mag.jpg | Kimura disease - intermed. mag. (WC)
</gallery>


==IHC==
==IHC==

Latest revision as of 03:01, 31 October 2015

Kimura disease
Diagnosis in short

Kimura disease. H&E stain.

LM eosinophils and thick walled blood vessels with hobnailed endothelial cells
LM DDx angiolymphoid hyperplasia with eosinophilia, drug reaction, infection (parasitic), lymphoma, LCH
Site lymph node, head and neck

Prevalence extremely rare
Blood work eosinophilia

Kimura disease is a rare disease with abundant eosinophils. It may show-up in a lymph node specimen. It is similar to angiolymphoid hyperplasia with eosinophilia.[1]

General

  • AKA eosinophilic lymphogranuloma, Kimura disease.
  • Chronic inflammatory disorder - suspected to be infectious.

Clinical:

  • Usually neck, periauricular.
  • Peripheral blood eosinophilia.
  • Increased blood IgE.

Epidemiology

  • Males > females.
  • Young.
  • Asian.

Microscopic

Features:[2]

  • Angiolymphoid proliferation.
    • Thick walled blood vessels with (plump) hobnail endothelial cells.[3]
  • Eosinophils - abundant - key feature.

DDx:

Notes:

  • In a lymph node... it may be signed-out as reactive lymphadenitis with follicular hyperplasia and prominent eosinophils, see comment.
  • Abundant eosinophils: consider Langerhans cell histiocytosis.

Images

IHC

  • Used to rule-out a clonal population, i.e. lymphoma.

See also

References

  1. URL: http://emedicine.medscape.com/article/1082603-overview. Accessed on: 14 January 2012.
  2. Ioachim, Harry L; Medeiros, L. Jeffrey (2008). Ioachim's Lymph Node Pathology (4th ed.). Lippincott Williams & Wilkins. pp. 190. ISBN 978-0781775960.
  3. URL: http://emedicine.medscape.com/article/1098777-diagnosis. Accessed on: 8 August 2010.