scholarly journals Bilateral sequential knee dislocation in a patient with connective tissue disorder: Report of an unusual case and lessons learnt

2016 ◽  
Vol 7 ◽  
pp. 41-44 ◽  
Author(s):  
Waheeb Al-Azzani ◽  
Konrad Wronka ◽  
James Lewis ◽  
Adel Ghandour ◽  
Angus Robertson
1960 ◽  
Vol XXXIII (IV) ◽  
pp. 613-622 ◽  
Author(s):  
B.-A. Lamberg ◽  
O. Wegelius ◽  
B. Kuhlbäck ◽  
C. Olin-Lamberg

ABSTRACT A case is described of a man of 48, who presented a history and clinical picture of a solitary thyro-hypophysial syndrome with malignant exophthalmos but in which general connective tissue changes were found on histological and histochemical examination of the retrobulbar connective tissue and muscles, of the pretibial connective and muscle tissue and the nasal epithelium. The intraocular tension was increased. In addition, renal failure developed. The use of cortisol locally in the eyes had a beneficial effect on the eye syndrome. Systemic treatment with corticotrophin and prednisolone had an evident beneficial effect on the renal condition.


2019 ◽  
Vol 12 (10) ◽  
pp. e231899
Author(s):  
Yinglun Wu ◽  
Philip C Dittmar

Rheumatoid arthritis (RA) is a common connective tissue disorder affecting the synovial joints. In patients with RA, involvement of the lungs occurs in 30%–40% of cases while pleural effusions occur in only 3%–5%. However, the majority of RA-associated pleural effusions are small, unilateral and asymptomatic. We present a case of massive bilateral pleural effusions in a patient with established rheumatoid pneumoconiosis (Caplan syndrome). Interestingly, the pleural effusion occurred following recent treatment for minimal change disease and atrial fibrillation.


1995 ◽  
Vol 83 (3) ◽  
pp. 546-549 ◽  
Author(s):  
Wouter I. Schievink ◽  
David G. Piepgras ◽  
Douglas A. Nichols

✓ The authors report a case of a 45-year-old woman with pulsatile tinnitus who was found to have an unusual spontaneous fistula between the petrous internal carotid artery and internal jugular vein. The fistula resolved spontaneously, possibly related to daily manual compression of the ipsilateral common carotid artery. The patient also had a contralateral carotid artery dissection, multiple intracranial arachnoid cysts, and hemifacial atrophy. Her medical history was significant for easy bruisibility, abnormal scarring, and mitral valve prolapse. This association appears unique and may represent a previously undescribed generalized connective tissue disorder.


2021 ◽  
pp. 1-3
Author(s):  
Willa Li ◽  
William Cohen ◽  
Pamela Combs ◽  
Joshua Wong ◽  
Rohit Loomba ◽  
...  

Abstract Loeys–Dietz syndrome is a connective tissue disorder known to cause aggressive aortopathy in paediatric patients, but it is extremely rare for cardiovascular events to present during infancy. We report the first successful aortic repair in a neonate with LDS presenting in extremis with an early onset, massive aortic aneurysm.


2021 ◽  
Author(s):  
Jennifer Hanson ◽  
Daniel Brezavar ◽  
Susan Hughes ◽  
Shivarajan Amudhavalli ◽  
Emily Fleming ◽  
...  

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