Closure of Thoracic and Lumbar Dysgraphic Defects Using Bilateral Latissimus Dorsi Myocutaneous Flap Transfer with Extended Gluteal Fasciocutaneous Flaps

1982 ◽  
Vol 9 (6) ◽  
pp. 394-399 ◽  
Author(s):  
N.B. McDevitt ◽  
R.P. Gillespie ◽  
R.E. Woosley ◽  
J.J. Whitt ◽  
A.G. Bevin
2007 ◽  
Vol 16 (1) ◽  
pp. 84-90 ◽  
Author(s):  
Kenji Kawamura ◽  
Hiroshi Yajima ◽  
Yasuharu Tomita ◽  
Yasunori Kobata ◽  
Koji Shigematsu ◽  
...  

2021 ◽  
Vol 48 (5) ◽  
pp. 494-497
Author(s):  
Byungkwon Kang ◽  
Yujin Myung

Bronchopleural fistula is a severe complication with a high mortality rate that occurs after pulmonary resection. Several treatment options have been suggested; however, it is a challenge to treat this condition without recurrence or other complications. In this case report, we describe the successful performance of a pedicled latissimus dorsi myocutaneous flap transfer, with no recurrence or donor site morbidity.


2002 ◽  
Vol 10 (2) ◽  
pp. 206-209 ◽  
Author(s):  
Y Taniguchi ◽  
T Tamaki ◽  
M Yoshida ◽  
Y Uematsu

A 53-year-old male underwent more than 10 surgical treatments over 14 years, including a simple excision and local flap transfer, after recurrences of dermatofibrosarcoma protuberans of the head. Clinical results indicated that simple excision of dermatofibrosarcoma protuberans should not be performed as initial treatment. Instead, free flap transplantation, which permits a wide excision and complete reconstruction, should be the first treatment option.


2020 ◽  
Vol 6 ◽  
pp. 2513826X1989883
Author(s):  
Sarah L. Zhu ◽  
David Choi ◽  
Jenny Santos ◽  
Bernard S. Jackson ◽  
Matthew McRae

This is the first report of pilomatrix carcinoma in a man with C282Y myotonic dystrophy type 1. This pilomatrix carcinoma had originally presented as a rapidly growing recurrence of a histopathologically confirmed pilomatrixoma, removed a year prior. On examination, the fungating mass had measured 10 × 23 cm. A wide local resection with removal of suspicious lymph nodes was preformed, and the resulting defect was reconstructed with a latissimus dorsi myocutaneous flap and skin graft. Histologic investigation of the excised mass confirmed the diagnosis of pilomatrix carcinoma. This is the first reported case of pilomatrix carcinoma in a patient with a genetic condition that often presents with scalp pilomatrixomas. Potential implications of myotonic dystrophy on developing pilomatrix carcinoma are discussed.


2013 ◽  
Vol 132 (4) ◽  
pp. 737-748 ◽  
Author(s):  
Olivier A. Branford ◽  
Noemi Kelemen ◽  
Christoph E. A. Hartmann ◽  
Rachel Holt ◽  
David Floyd

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