Giant cell arteritis without clinically evident vascular involvement in a defined population

Wiley - Tập 51 Số 2 - Trang 274-277 - 2004
Miguel Á. González‐Gay1, Carlos García‐Porrúa1, Juan Carlos Amor-Dorado1, Javier Llorca2
1Hospital Xeral Calde, Lugo, Spain
2School of Medicine, University of Cantabria, Santander, Spain

Tóm tắt

AbstractObjectives

To examine the frequency and clinical presentation of biopsy‐proven giant cell arteritis (GCA) patients who do not exhibit overt clinical vascular manifestations. To assess whether differences exist between this group of patients and the rest of biopsy‐proven GCA patients.

Methods

Retrospective study of biopsy‐proven GCA patients diagnosed from 1981 through 2001 at the single hospital for a well‐defined population of almost 250,000 people. Patients were considered as having no evident vascular involvement if cranial ischemic manifestations or other vascular complications of GCA were not present at the time of diagnosis or during at least 12 months' followup.

Results

Between 1981 and 2001, 210 patients from the Lugo region of northwest Spain were diagnosed with biopsy‐proven GCA. Eleven patients did not show overt vascular manifestations of GCA. Nine of them presented with polymyalgia rheumatica (PMR) and another 2 fulfilled criteria for fever of unknown origin. Patients without clinically evident vascular involvement had a significantly longer delay to diagnosis than those with vascular manifestations. Also, PMR manifestations were more frequently observed in this group of patients.

Conclusions

Biopsy‐proven GCA without clinically evident vascular involvement is not exceptional. Despite having a longer delay to diagnosis, these patients constitute a more benign subgroup of GCA.

Từ khóa


Tài liệu tham khảo

10.1016/S0889-857X(05)70232-5

10.1002/art.1780230605

10.1002/art.1780241113

10.1111/j.1365-2796.1990.tb00151.x

10.1097/00005792-199909000-00002

10.1097/00005792-200009000-00001

Gonzalez‐Gay MA, 1999, The spectrum of polymyalgia rheumatica in Northwestern Spain: incidence and analysis of variables associated with relapse in a ten year study, J Rheumatol, 26, 1326

10.7326/0003-4819-97-5-672

10.1097/00005792-199711000-00002

10.1002/art.1780370411

10.1186/ar293

Gonzalez‐Gay MA, 1998, Polymyalgia rheumatica in biopsy‐proven giant cell arteritis does not constitute a different subset but differs from isolated polymyalgia rheumatica, J Rheumatol, 25, 1750

10.1136/ard.60.4.367

Amoli MM, 2002, Intercellular adhesion molecule‐1 gene polymorphisms in isolated polymyalgia rheumatica, J Rheumatol, 29, 502

10.1111/j.1532-5415.1978.tb03333.x

10.1016/S0140-6736(80)90675-3

10.1002/1529-0131(199801)41:1<26::AID-ART4>3.0.CO;2-0

10.1002/1529-0131(200006)43:6<1427::AID-ANR35>3.0.CO;2-P

10.1016/S0002-9440(10)65175-9

10.1161/01.CIR.0000030185.67510.C0