Rheumatoid Arthritis and CLOVES Syndrome: A Tricky Diagnosis

被引:7
作者
Damian, Laura [1 ,2 ]
Lebovici, Andrei [3 ]
Pamfil, Cristina [4 ]
Belizna, Cristina [5 ,6 ]
Vulturar, Romana [7 ,8 ]
机构
[1] Cab Reumatol Dr Damian, 6-8 Petru Maior St, Cluj Napoca 400002, Romania
[2] Emergency Clin Cty Hosp Cluj, Rheumatol Dept, Ctr Rare Musculoskeletal Autoimmune & Autoinflamm, 2-4 Clinicilor St, Cluj Napoca 400006, Romania
[3] Iuliu Hatieganu Univ Med & Pharm Cluj, Radiol Dept, 8 Victor Babes St, Cluj Napoca 400023, Romania
[4] Iuliu Hatieganu Univ Med & Pharm Cluj, Ctr Rare Musculoskeletal Autoimmune & Autoinflamm, 8 Victor Babes St, Cluj Napoca 400023, Romania
[5] Univ Hosp Angers, Vasc & Coagulat Dept, F-49100 Angers, France
[6] CNRS, INSERM, U1083, UMR 6015, Rue Haute Reculee, F-40945 Angers 01, France
[7] Iuliu Hatieganu Univ Med & Pharm Cluj, Dept Mol Sci, 6 Pasteur St, Cluj Napoca 400349, Romania
[8] Univ Babes Bolyai, Cognit Neurosci Lab, 30 Fantanele St, Cluj Napoca 400294, Romania
关键词
CLOVES syndrome; rheumatoid arthritis; macrodactyly; PIK3/AKT/mTOR pathway; PIK3CA-related overgrowth spectrum; RAPAMYCIN; PATIENT; TARGET; DELTA;
D O I
10.3390/diagnostics10070467
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The PI3K/AKT/mTOR signaling pathway is significantly activated in rheumatoid arthritis. In addition, somatic activating mutations of the PI3K/AKT/mTOR pathway may result inPIK3CA-related overgrowth spectrum diseases, including CLOVES (Congenital Lipomatous Overgrowth, Vascular malformation, Epidermal nevi, Skeletal abnormalities/Scoliosis) syndrome. We describe the case of a young female patient, with anti-citrullinated peptide antibodies-positive rheumatoid arthritis, referred for persistent finger pain and stiffness. Examination revealed discrete macrodactyly involving two fingers, scoliosis, asymmetrical calves, venectasias, a shoulder nevus and triangular feet with a "sandal gap" between two toes. These mild dysmorphic features with early-onset and the history of surgeries for thoracic lipoma and venous malformation were strongly suggestive of CLOVES syndrome. Confirmatory mutation analysis was not performed, as blood or saliva testing is not contributive for tissue-specific localized effects in thePIK3CA-related overgrowth spectrum. Nevertheless, lack of detection of aPIK3CAmutation does not exclude the diagnosis in patients fulfilling clinical criteria. Due to the patient's wish to plan a pregnancy, therapy consisted in sulfasalazine and hydroxychloroquine, along with orthotic correction of leg length discrepancy. Overgrowth syndromes and arthritis may share common pathways. Mild macrodactyly should be differentiated from dactylitis. Diagnosing patients with minimal dysmorphic features within the PI3K-related overgrowth spectrum may help design better care strategies, in the quest for personalized medicine.
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页数:5
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