Long-term outcome after surgical excision of parenchymal arteriovenous malformations in patients over 60 years of age

1997 ◽  
Vol 47 (3) ◽  
pp. 258-263 ◽  
Author(s):  
Giuseppe Lanzino ◽  
Allan H. Fergus ◽  
Mary E. Jensen ◽  
Gail L. Kongable ◽  
Neal F. Kassell
2014 ◽  
Vol 37 (5) ◽  
pp. 342-349 ◽  
Author(s):  
Yu-Chi Wang ◽  
Yin-Cheng Huang ◽  
Hsien-Chih Chen ◽  
Kuo-Cheng Wei ◽  
Cheng-Nen Chang ◽  
...  

2007 ◽  
Vol 32 (5) ◽  
pp. 502-508 ◽  
Author(s):  
J. J. DIAS ◽  
V. DHUKARAM ◽  
P. KUMAR

We have evaluated the long-term outcome of excision, aspiration and no treatment of dorsal wrist ganglia prospectively in 236 (83%) of 283 patients who responded to a postal questionnaire at a mean of 70 months. The resolution of symptoms was similar between the treatment groups ( p>0.3). Pain and unsightliness improved in all three treatment groups. The prevalence of weakness and stiffness altered only slightly in all three treatment groups. More patients with a recurrent, or persistent ganglion complained of pain, stiffness and unsightliness ( p<0.0001). Patient satisfaction was higher after surgical excision ( p<0.0001), even if the ganglion recurred. Twenty-three of 55 (58%) untreated ganglia resolved spontaneously. The recurrence rate was 58% (45/78) and 39% (40/103) following aspiration and excision, respectively. Eight out of 103 patients had complications following surgery. In this study, neither excision nor aspiration provided significant long-term benefit over no treatment.


2016 ◽  
Vol 6 (21) ◽  
pp. 49-51
Author(s):  
Dan Cristian Gheorghe ◽  
Adina Zamfir-Chiru-Anton

Abstract Tumors of the maxillary sinus pose difficult challenges in a young patient. Our paper presents a very rare case of an odontogenic myxoma extended to the maxillary sinus, in a 14-year-old girl. The clinical picture suggested a malignancy or a local infection. The surgical removal was complete and the diagnosis was confirmed by immunohistochemistry. Discussions are made from the perspective of already published cases. A review of the disease is performed. CONCLUSION. Myxoma is a benign but aggressive tumor, needing complete surgical excision for a good long-term outcome.


2017 ◽  
Vol 5 ◽  
pp. 2050313X1774051
Author(s):  
Dean J Samaras ◽  
Andrew C Kingsford

Extensive hypertrophic scarring of the halluces secondary to chronic onychocryptosis is a rare condition, which causes significant physical and psychosocial effects. In this case, a 31-year-old male developed large lesions on both great toes after he delayed treatment of chronic hallucal onychocryptosis for over a decade. Current treatment options for hypertrophic and keloid lesions in the foot and ankle vary considerably and differentiation is critical for appropriate treatment planning. In this case, surgical excision with total matrixectomy (modified Zadik–Syme) was considered optimal management. Histopathology testing confirmed the diagnosis of irritated hypertrophic scar secondary to onychocryptosis. The patient was monitored closely and at 3 months post-operatively, the incisional scars exhibited progressive maturation, and there was no recurrence of the lesions and no nail regrowth. Furthermore, the halluces were only marginally shorter providing good function and cosmesis. At the long-term follow-up consultation (5.5 years), the patient indicated complete satisfaction and had returned to regular footwear and social activities. Chronic onychocryptosis can trigger and facilitate proliferation of large benign keloid-like fibrous lesions; excision with total matrixectomy can provide an excellent long-term outcome.


1993 ◽  
Vol 79 (2) ◽  
pp. 270-276 ◽  
Author(s):  
Adam N. Mamelak ◽  
William M. Kelly ◽  
Richard L. Davis ◽  
Mark L. Rosenblum

✓ Hypertrophic cranial pachymeningitis is a rare, idiopathic form of granulomatous pachymeningitis. This report describes three cases of hypertrophic cranial pachymeningitis and discusses the clinical, radiographic, and pathological findings in these and other reported cases. These lesions typically cause progressive cranial nerve palsies, headaches, and cerebellar dysfunction. They occur in patients of all age groups; the peak incidence is in the sixth decade. Hypertrophic cranial pachymeningitis is best identified by magnetic resonance imaging. The diagnosis is established by excluding all other granulomatous and infectious diseases. A dural biopsy is essential to confirm the diagnosis. Hypertrophic cranial pachymeningitis is initially responsive to steroid therapy, but in most cases it recurs or progresses despite treatment. Surgical excision of granulomas is occasionally necessary to alleviate a mass effect. The long-term outcome remains uncertain for most patients, but progressive disease is usually fatal owing to cranial neuropathies.


2012 ◽  
Vol 24 ◽  
pp. 126-129 ◽  
Author(s):  
Gigi Thomas ◽  
Ramadas Kunnambath ◽  
Thara Somanathan ◽  
Babu Mathew ◽  
Manoj Pandey ◽  
...  

2000 ◽  
Vol 11 (10) ◽  
pp. 1285-1295 ◽  
Author(s):  
Robert I. White ◽  
Jeffrey Pollak ◽  
John Persing ◽  
Katharine J. Henderson ◽  
J. Grant Thomson ◽  
...  

Neurosurgery ◽  
2018 ◽  
Vol 84 (1) ◽  
pp. 151-159 ◽  
Author(s):  
Elias Oulasvirta ◽  
Päivi Koroknay-Pál ◽  
Ahmad Hafez ◽  
Ahmed Abou Elseoud ◽  
Hanna Lehto ◽  
...  

Stroke ◽  
2014 ◽  
Vol 45 (6) ◽  
pp. 1664-1671 ◽  
Author(s):  
Thomas Blauwblomme ◽  
Marie Bourgeois ◽  
Philippe Meyer ◽  
Stéphanie Puget ◽  
Federico Di Rocco ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document