Journals / Türkderm-Deri Hastalıkları ve Frengi Arşivi / 2009 / Cilt: 43 - Sayı: 3

Angiolymphoid hyperplasia with eosinophilia: A case report

Eozinofilili anjiolenfoid hiperplazi: Bir olgu sunumu

Pages
119–121
Publication Date
2022-11-05
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Rather, destructive methods have been used for therapy, including electrodessication, cryotherapy, surgical excision, radiotherapy, intralesionary therapy (sclerosing or glucocorticoid), interferon-a2a, cytotoxic agents, pentoxifilin, pulse dye lazer, argon laser and CO2 laser.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Angiolymphoid hyperplasia with eosinophilia is a rare disorder characterized by vascular proliferation, eosinophilia in peripheral blood and lymphocytosis.
📊
Key Findings & Data:With unknown etiology, this rare condition is generally seen in women.
💡
Conclusion & Impact:Rather, destructive methods have been used for therapy, including electrodessication, cryotherapy, surgical excision, radiotherapy, intralesionary therapy (sclerosing or glucocorticoid), interferon-a2a, cytotoxic agents, pentoxifilin, pulse dye lazer, argon laser and CO2 laser.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Angiolymphoid hyperplasia with eosinophilia is a rare disorder characterized by vascular proliferation, eosinophilia in peripheral blood and lymphocytosis. With unknown etiology, this rare condition is generally seen in women. It often presents as multiple, grouped red nodules in the peri-auricular region, scalp line and neck. Although it is limited, spontaneous resolution may be seen in lesions. Rather, destructive methods have been used for therapy, including electrodessication, cryotherapy, surgical excision, radiotherapy, intralesionary therapy (sclerosing or glucocorticoid), interferon-a2a, cytotoxic agents, pentoxifilin, pulse dye lazer, argon laser and CO2 laser.

Özet

Eozinofilili anjiolenfoid hiperplazi, periferik kanda eozinofili ve lenfositoz ile birlikte vasküler proliferasyonla karakterize nadir bir hastalıktır. Etyolojisi bilinmeyen bu nadir durum genellikle kadınlarda görülmektedir. Sıklıkla peri-aurikular bölge, saçlı deri ve boyunda çok sayıda, grube kırmızı nodüllerle karşımıza çıkar. Çoğunlukla kendi kendini sınırlar ve lezyonlar kendiliğinden gerileyebilir. Tedavisinde elektrodesikasyon, kriyoterapi, cerrahi eksizyon, radyoterapi, intralezyoner tedavi (sklerozan ya da steroid), interferon-a2a, sitotoksik ajanlar, pentoksifilin, pulse dye lazer, argon lazer, CO2 lazer gibi daha çok destrüktif tedavi yöntemleri kullanılmaktadır.

🔖

Cite This Article

GENÇOĞLAN, G., CEYLAN, C., ŞAHİN, S., ERTEKİN, B., KAZANDI, A. C. (2022). Angiolymphoid hyperplasia with eosinophilia: A case report. Türkderm-Deri Hastalıkları ve Frengi Arşivi, Cilt: 43 - Sayı: 3, 119–121. https://ajindex.com/articles/622397

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (15)

  1. Requena L, Sangueza OP. Cutaneous vascular proliferation part 2. Hyperplasias and benign neoplasms. J Am Acad Dermatol 1997;37:887-920
  2. Selim Vasküler Tümörler. Baykal C. Dermatoloji Atlası, 2. baskı, ‹stanbul: Argos 2004;570-1
  3. Braun-Falco O, Plewing G, Wolff HH, Burgdorf WHC. Angiolymphoid hyperplasia with eosinophilia. In: Dermatology, second Ed. Berlin, Springer-Verlag 2000:1553-601
  4. Mansur TA, Serdar ZA, Kılıç Z, Aydıngöz ‹E, Yıldız K. Eozinofilili Anjiolenfoid Hiperplazi: Bir Olgu Sunumu. T Klin J Dermatol 2004;14:38-43
  5. Arnold M, Geilen CC, Coupland SE, Krengel S, Dippel E, Sproder J, Goerdt S, Orfanos CE. Unilateral angiolymphoid hyperplasia with eosinophilia involving the left arm and hand. J Cutan Pathol 1999;26:436-40
  6. Blauvelt A, Cobb MW, Turner ML. Widespread cutaneous vascular papules associated with peripheral blood eosinophilia and prominent inguinal lymphadenopathy. J Am Acad Dermatol 2000;43:698-700
  7. Onishi Y, Ohara K. ALHE associated with arteriovenous malformation: a clinicopathological correlation with angiography and serial estimation of serum levels of renin, eosinophil cationic protein and interleukin 5. Br J Dermatol 1999;140:1153-6
  8. Misago N, Tanaka T, Kodera H, Narisawa Y: Localized soft tissue angiomatosis with subsequent development of ALHE. J Dermatol 1999;26:48-55
  9. Aoki M, Kimura Y, Kusunoki T, Tahara S, Kawanah S. Angiolymphoid hyperplasia with eosinophilia associated with anomalous dilatation of occipital artery: IL-5 and VEGF expression of lesional mast cells. Arch Dermatol 2002;138:982-4
  10. Chun SI, Ji HG. Kimura's disease and angiolymphoid hyperplasia with eosinophilia: clinical and histopathologic differences. J Am Acad Dermatol. 1992;27:954-8
  11. Helander SD, Peters MS, Kuo TT, Su WP. Kimura’s disease and angiolymphoid hyperplasia with eosinophilia: New observations from immunohistochemical studies of lymphocyte markers, endothelial antigens and granulocyte proteins. J Cutan Pathol 1995;22:319-26
  12. Baykal C, Beyazıt Ö, Büyükbabani N. Erüptif anjiyomatöz lezyonlarda etyopatogenez ve ayırıcı tanı. Turk J Dermatopathol 1995;3:147-55
  13. Gencoglan G, Karaca S, Ertekin B. Angiolymphoid hyperplasia with eosinophilia successfully treated with imiquimod. A case report. Dermatology. 2007;215:233-5
  14. Redondo P, Olmo JD, Idoate M. Angiolymphoid hyperplasia with eosinophilia succesfully treated with imiquimod. British Journal of Dermatology 2004;151:1110
  15. Kaur T, Sandhu K, Gupta S, Kanwar A