Journals / Acıbadem Üniversitesi Sağlık Bilimleri Dergisi / 2014 / Sayı: 3

Answer To “what Is Your Diagnosis?” On P.198

Answer to “What is Your Diagnosis?” on p.198

Pages
236–237
Publication Date
2014-09-01
DOI
—
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AI Summary & Key Takeaways

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

However, in our patient lack of true blisters, milia, scarring, and the negative urine test in addition to positive staining with Congo red and amyloid P eliminated porphyria

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Öz seen on the pretibial surfaces, a clinical picture highly different from ACM 4 .
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Key Findings & Data:The clinical features of nodu- lar amyloidosis with waxy, smooth papules, nodules or plaques on the face, trunk, or genitalia are also characteristic enough to distinguish it from ACM 2 .
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Conclusion & Impact:However, in our patient lack of true blisters, milia, scarring, and the negative urine test in addition to positive staining with Congo red and amyloid P eliminated porphyria
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Öz seen on the pretibial surfaces, a clinical picture highly different from ACM 4 . The clinical features of nodu- lar amyloidosis with waxy, smooth papules, nodules or plaques on the face, trunk, or genitalia are also characteristic enough to distinguish it from ACM 2 . Acral persistent papular mucinosis may be confused with ACM, because of the presence of multiple, skin coloured papules localized to the hands and wrists. Alcian blue staining is a definite marker for its diag- nosis 5 . Disorders of porphyrin metabolism may be considered in the differential diagnosis of ACM, due to the involvement of sun-exposed areas 1 . However, in our patient lack of true blisters, milia, scarring, and the negative urine test in addition to positive staining with Congo red and amyloid P eliminated porphyria

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Cite This Article

MANSUR, A. T. (2014). Answer To “what Is Your Diagnosis?” On P.198. Acıbadem Üniversitesi Sağlık Bilimleri Dergisi, Sayı: 3, 236–237. https://ajindex.com/articles/163013

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References (5)

  1. Pourrabbani S, Marra DE, Iwasaki J, Fincher EF, Ronald LM. Colloid milium: a review and update. J Drugs Dermatol 2007; 6: 293-6.
  2. Desai AM, Pielop JA, Smith-Zagone MJ, Hsu S. Colloid milium: A histopathologic mimicker of nodular amyloidosis. Arch Dermatol 2006; 142: 784-5.
  3. Rangioletti F, Barnhill RL. Deposition disorders in Dermatopathology. Eds. Barnhill RL, Crowson AN, Magro CM, Piepkorn MW. 3rd ed, 2010,
  4. Mc Graw Hill Medical, New York, pp.378-9. al-Ratrout JT, Satti MB. Primary localized cutaneous amyloidosis: a clinicopathologic study from Saudi Arabia. Int J Dermatol 1997; 36: 428-34.
  5. Harris JE, Purcell SM, Griffin TD. Acral persistent papular mucinosis. J Am Acad Dermatol 2004; 51: 982-8.