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Case report: Diagnostic challenges of papulonodular mucinosis in a 67-year-old female
被引:0
|作者:
Loreman, Holly E. Zahary
[1
]
Holfeld, Karen, I
[2
]
机构:
[1] Univ Calgary, Cumming Sch Med, 115-3130 Thirsk Street NW, Calgary, AB T3B6H4, Canada
[2] Univ Saskatchewan, Coll Med, Div Dermatol, Saskatoon, SK, Canada
来源:
关键词:
Mucinosis;
papulonodular mucinosis;
papular and nodular mucinosis of Gold;
cutaneous lupus mucinosis;
lupus erythematosus;
dermatopathology;
hydroxychloroquine;
D O I:
10.1177/2050313X241311372
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Papulonodular mucinosis is a rare dermatological condition characterized by mucin deposition in the dermis, leading to the formation of papules and nodules that can occur with, or antedate, autoimmune connective tissue diseases. This case report presents a 67-year-old female with a chronic history of cutaneous mucinosis, which posed significant diagnostic challenges. Despite various treatments and extensive diagnostic workup, her condition evolved, highlighting the difficulties in diagnosing papulonodular mucinosis, especially in the absence of systemic lupus erythematosus and antinuclear antibody positivity. The unusual presentation and diagnostic complexity underscore the need for awareness and thorough investigation in similar cases.
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