## Abstract ## Background. Eightyβfive percent of all Merkel cell carcinomas appear on sunβexposed areas, with 50% to 55% occurring on the head and neck. ## Methods. A chart review was performed on 22 patients treated for Merkel cell carcinoma of the head and neck between 1981 and 1998. ## Resu
Lymphatic malformations of the head and neck: A retrospective review and a support for staging
β Scribed by Marc Hamoir; Isabelle Plouin-Gaudon; Philippe Rombaux; Genevieve Francois; Anne-Sophie Cornu; Gauthier Desuter; Philippe Clapuyt; Christian Debauche; Gaston Verellen; Claire Beguin
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 614 KB
- Volume
- 23
- Category
- Article
- ISSN
- 1043-3074
- DOI
- 10.1002/hed.1039
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Background
Lymphatic malformations (LM) are rare benign congenital tumors appearing mainly in the head and neck with a considerably variable outcome. A need exists to validate a staging system, taking into account the prognosis of the malformation, including preoperative and postoperative complications, longβterm sequelae, and persistence of the disease to improve parental counseling and evaluate the outcome of a surgical treatment of such tumors.
Methods
Twentyβtwo patients treated for LM were selected from a series of 129 patients operated on for congenital malformations of the head and neck between 1986 and 1997 at StβLuc University Hospital, Brussels, Belgium. Their charts were reviewed retrospectively, with a special focus on the anatomic location of the lesions and all the complications reported. According to de Serres et al, LM up to now have been divided into six possible categories according to their unilateral or bilateral infrahyoid and/or suprahyoid locations.
Results
Stage I (unilateral infrahyoid): nine patients, 11% of complications (without mediastinal extension: 0%, with mediastinal extension: 50%); stage II (unilateral suprahyoid): three patients, 33% of complications; stage III (unilateral suprahyoid and infrahyoid): eight patients, 75% of complications; stage V (bilateral suprahyoid and infrahyoid): two patients, 100% of complications. None of the children was initially seen with stage IV (bilateral suprahyoid) or stage VI (bilateral infrahyoid) LM. Overall complications, preoperative complications, postoperative comβ plications, and longβterm morbidity showed a significant inβ crease from stage I to V (p < .01, p = .002, p = .02, and p = .03, respectively).
Conclusions
A staging system of cervicofacial LM based on the anatomic location can be reliably used for prognostic purposes, allowing a more accurate assessment of the global risk of complications and determination of surgical outcome. Mediastinal extension in stage I patients seems to be associated with a higher rate of complications. Such information can be used to inform parents more appropriately regarding the management and longβterm prognosis of their children's malformation. Β© 2001 John Wiley & Sons, Inc. Head Neck 23: 326β337, 2001.
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