scholarly journals O015 / #550: OVERLAPPING IMMUNE-SIGNATURE AMONG ACUTE NEURO-IMMUNE DISORDERS AND PSYCHOTIC DISORDERS IN ADOLESCENTS AND YOUNG ADULTS; A CASE SERIES.

2021 ◽  
Vol 22 (Supplement 1 3S) ◽  
pp. 10-10
Author(s):  
N. Chiriboga ◽  
M. Kerrigan ◽  
L. Peters ◽  
T. Brusko ◽  
D. Perry ◽  
...  
2014 ◽  
Vol 70 (2) ◽  
pp. 388-390 ◽  
Author(s):  
Bianca Maria Piraccini ◽  
Bertrand Richert ◽  
David A. de Berker ◽  
Vera Tengattini ◽  
Paola Sgubbi ◽  
...  

2017 ◽  
Vol 136 (2) ◽  
pp. 188-200 ◽  
Author(s):  
M. Lambert ◽  
D. Schöttle ◽  
F. Ruppelt ◽  
A. Rohenkohl ◽  
M. Sengutta ◽  
...  

Addiction ◽  
2010 ◽  
Vol 105 (9) ◽  
pp. 1669-1676 ◽  
Author(s):  
Marc J. Fishman ◽  
Erin L. Winstanley ◽  
Erin Curran ◽  
Shannon Garrett ◽  
Geetha Subramaniam

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Kiran Kumar Ganji ◽  
ArunKumar Bhimashankar Chakki ◽  
Sharanbasappa Chandrashekar Nagaral ◽  
Esha Verma

The concept of fibroosseous lesions of bone has evolved over the last several decades and now includes two major entities: fibrous dysplasia and ossifying fibroma. Peripheral cemento-ossifying fibroma is a relatively rare tumour classified between fibroosseous lesions. It predominantly affects adolescents and young adults, with peak prevalence between 10 and 19 yrs. The cemento-ossifying fibroma is a central neoplasm of bone as well as periodontium which has caused considerable controversy because of confusion regarding terminology and the criteria for its diagnosis. The cemento-ossifying fibroma is odontogenic in origin, whereas ossifying fibroma is of bony origin. Lesions histologically similar to peripheral ossifying fibroma have been given various names in existing literature. Therefore, we present and discuss in this paper a series of cases of peripheral cemento-ossifying fibroma emphasizing the differential diagnosis.


2019 ◽  
Vol 25 (3) ◽  
pp. 84-89
Author(s):  
D. Keshet ◽  
S. Salminen ◽  
M. Eidelman

Introduction. Brachymetatarsia is a relatively rare abnormal shortening of metatarsal bone with female predominance. No consensus exists about the ideal surgical treatment for this condition while the two common strategies are gradual lengthening using external fixation and acute one stage lengthening. We describe the surgical technique of acute lengthening using iliac bone graft and report our results. Materials and Methods. Twelve patients (11 females, one male) with 14 short metatarsals were treated in our hospital over a 12-year period. The mean age was 17.4 years (range 14-28 years). Treatment protocol included metatarsal osteotomy, lengthening of extensor tendon and percutaneous tenotomy of the flexor tendon at the level of affected MP joint. Autologous iliac bone graft was inserted after elongation of the metatarsal by distraction through the osteotomy site and fixed using Kirshner wire. Results. Average metatarsal shortening was 13mm (range, 11-18 mm). The metatarsal length gained was an average of 12mm (range, 11-15 mm). Uneventful bone union was achieved in all cases after six weeks. At the end of treatment, the normal cascade of the metatarsal heads (metatarsal parabola) had been restored in 11 of the 14 metatarsals treated. There were no wound complications or pin tract infections around the wire. All but one patient were satisfied with the cosmetic appearance of the foot. Conclusion. Based on our experience, acute metatarsal lengthening using an iliac autugraft is a reliable and effective treatment method for congenital brachymetatarsia in adolescents and young adults.Level of Evidence: Level IV Case series.


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