
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions โ written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Caplans syndrome natural history, complications and prognosis
Introduction
Overview
Overview
If left untreated, some patients might develop irreversible pulmonary fibrosis.
Natural History, Complications, and Prognosis
Natural History, Complications, and Prognosis
Natural History
- The patients with Caplan syndrome are mostly asymptomatic initially. [1] [2]
- Caplan nodules appear with or later than the onset of Rheumatoid arthritis.[3]
- Caplan nodules may lead to cavitation or calcification with pleural effusion or in rare cases pneumothorax.
- Lung nodules in Caplan syndrome are rapidly growing; gain final size within weeks to month and then remain unchanged for years long.
- Most of the lung nodules resolve spontaneously while some leave behind asteroid scarring. In 10% cases, cavitation and calcification happen.
- There are cases of Caplan syndrome with radiologic findings of Caplan nodules but no rheumatoid factor.
- The symptoms of dyspnea and cough typically develop with the progression of the disease.
- If left untreated, patients with Caplan syndrome may progress to develop wheeze in the chest which doesn’t change with cough suggestive of irreversible pulmonary fibrosis.
Complications
Possible complications include[3] [4]:
- Increased risk for tuberculosis and aspergillosis
- Hemoptysis
- Pleural effusion
- Pneumothorax
- Progressive massive fibrosis (scarring)
- Side effects of medications
Prognosis
Caplan syndrome rarely causes serious breathing trouble or disability due to lung problems.[4]
The nodules may pre-date the appearance of rheumatoid arthritis by several years. Otherwise, prognosis is as for RA; lung disease may remit spontaneously, but pulmonary fibrosis may also progress.
References
References
- โ Benedek, Thomas G. (1973). “Rheumatoid pneumoconiosis”. The American Journal of Medicine. 55 (4): 515โ524. doi:10.1016/0002-9343(73)90209-X. ISSNย 0002-9343.
- โ Alaya, Zeineb; Braham, Mouna; Aissa, Sana; Kalboussi, Houda; Bouajina, Elyรจs (2018). “A case of Caplan syndrome in a recently diagnosed patient with silicosis: A case report”. Radiology Case Reports. 13 (3): 663โ666. doi:10.1016/j.radcr.2018.03.004. ISSNย 1930-0433.
- โ 3.0 3.1 Lindars, D. C.; Davies, D. (1967). “Rheumatoid pneumoconiosis: A study in colliery populations in the East Midlands coalfield”. Thorax. 22 (6): 525โ532. doi:10.1136/thx.22.6.525. ISSNย 0040-6376.
- โ 4.0 4.1 Caplan, A.; Payne, R. B.; Withey, J. L. (1962). “A Broader Concept of Caplan’s Syndrome Related to Rheumatoid Factors”. Thorax. 17 (3): 205โ212. doi:10.1136/thx.17.3.205. ISSNย 0040-6376.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Sharmi Biswas, M.B.B.S
