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Papulonodular Mucinosis Associated With Subacute Lupus
Sabrine Rabba1, Fouzia Hali1, Farida Marnissi2
1Department of Dermatology, Ibn Rochd University Hospital, Casablanca, MAR.
Papulonodular mucinosis, a rare finding in lupus erythematosus, exceptionally occurred with subacute cutaneous lupus erythematosus (SCLE). This case highlights the need for close monitoring of patients with SCLE-associated mucinosis for systemic disease progression.
Area of Science:
- Dermatology
- Rheumatology
- Pathology
Background:
- Papulonodular mucinosis is a rare finding in lupus erythematosus (LE).
- It is exceptionally associated with subacute cutaneous lupus erythematosus (SCLE).
- The etiology and pathogenesis of papulonodular mucinosis remain unclear.
Observation:
- A middle-aged woman presented with asymptomatic flesh-colored papules and nodules on her trunk and upper extremities.
- A biopsy of a nodule revealed dermal and hypodermal mucin deposition.
- Perivascular lymphocytic inflammation was noted on histopathology.
Findings:
- This case documents papulonodular mucinosis in association with subacute cutaneous lupus erythematosus (SCLE).
- Histopathological examination confirmed mucin deposition and inflammation.
- The patient's presentation adds to the limited literature on this rare association.
Implications:
- The proportion of patients with cutaneous lupus mucinosis progressing to systemic lupus is uncertain.
- Close monitoring for multisystem disease is recommended for patients with SCLE-associated mucinosis.
- Further research into the pathogenesis of this rare condition is warranted.
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