Cutaneous nasal malignancies: is primary reconstruction safe?
Abstract
[BACKGROUND] The nose is particularly vulnerable to cutaneous malignancies, making it the most common location for presentation. Recurrence of these cutaneous lesions is not uncommon, often compromising the timing of nasal restoration. It is the purpose of this report to reexamine the safety of primary nasal reconstruction in selected patients.
[METHODS] Seventy-one patients who underwent nasal reconstruction at The University of Texas M. D. Anderson Cancer Center between 1987 and 1995 were retrospectively reviewed. There were 35 men and 36 women with an average age of 60 years. All nasal reconstructions were performed for defects secondary to malignancies. Basal cell carcinoma was the most common lesion (n = 49), followed by squamous cell carcinoma (n = 10) and melanoma (n = 7), with five additional variable malignancies. The most common location of the cutaneous lesions was the nasal dorsum, and the forehead flap was the most common adjacent tissue used for reconstruction. Immediate reconstruction was performed for 42 of the basal cell carcinomas, 6 of the squamous cell carcinomas, 6 melanomas, and 3 other lesions. Delayed restoration was performed for 7 basal cell carcinomas, 4 squamous cell carcinomas, 1 melanoma, and 2 additional lesions. The average time between surgical extirpation and the start of nasal reconstruction was 8.2 months for basal cell carcinoma, 29 months for squamous cell carcinoma, and 10 months for melanoma.
[RESULTS] Twenty-six recurrent lesions were identified at an average of 36 months after extirpation. Despite these numbers, only three recurred after nasal reconstruction at our institution. Follow-up averaged 41 months, with none less than 1 year. Seventy patients are still alive with no evidence of disease.
[CONCLUSION] Primary reconstruction is safe in selected patients. Surgical delay in reconstruction should be considered if margins are questionable, the pathology is determined to be aggressive, if there is perineural or deep bony invasion, or if postoperative radiotherapy is to be initiated. Nasal reconstruction ultimately is based upon a complex series of issues but can be performed with few complications in an effort to restore self-image.
[METHODS] Seventy-one patients who underwent nasal reconstruction at The University of Texas M. D. Anderson Cancer Center between 1987 and 1995 were retrospectively reviewed. There were 35 men and 36 women with an average age of 60 years. All nasal reconstructions were performed for defects secondary to malignancies. Basal cell carcinoma was the most common lesion (n = 49), followed by squamous cell carcinoma (n = 10) and melanoma (n = 7), with five additional variable malignancies. The most common location of the cutaneous lesions was the nasal dorsum, and the forehead flap was the most common adjacent tissue used for reconstruction. Immediate reconstruction was performed for 42 of the basal cell carcinomas, 6 of the squamous cell carcinomas, 6 melanomas, and 3 other lesions. Delayed restoration was performed for 7 basal cell carcinomas, 4 squamous cell carcinomas, 1 melanoma, and 2 additional lesions. The average time between surgical extirpation and the start of nasal reconstruction was 8.2 months for basal cell carcinoma, 29 months for squamous cell carcinoma, and 10 months for melanoma.
[RESULTS] Twenty-six recurrent lesions were identified at an average of 36 months after extirpation. Despite these numbers, only three recurred after nasal reconstruction at our institution. Follow-up averaged 41 months, with none less than 1 year. Seventy patients are still alive with no evidence of disease.
[CONCLUSION] Primary reconstruction is safe in selected patients. Surgical delay in reconstruction should be considered if margins are questionable, the pathology is determined to be aggressive, if there is perineural or deep bony invasion, or if postoperative radiotherapy is to be initiated. Nasal reconstruction ultimately is based upon a complex series of issues but can be performed with few complications in an effort to restore self-image.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 시술 | flap
|
피판재건술 | dict | 1 | |
| 해부 | nasal
|
scispacy | 1 | ||
| 해부 | cutaneous lesions
|
scispacy | 1 | ||
| 해부 | tissue
|
scispacy | 1 | ||
| 해부 | nasal dorsum
|
콧등 | dict | 1 | |
| 합병증 | nasal reconstructions
|
scispacy | 1 | ||
| 합병증 | forehead flap
|
scispacy | 1 | ||
| 합병증 | lesions
|
scispacy | 1 | ||
| 약물 | [BACKGROUND] The
|
scispacy | 1 | ||
| 질환 | malignancies
|
scispacy | 1 | ||
| 질환 | Cancer
|
scispacy | 1 | ||
| 질환 | disease
|
scispacy | 1 | ||
| 질환 | Cutaneous nasal malignancies
|
scispacy | 1 | ||
| 질환 | nose
|
C0028429
Nose
|
scispacy | 1 | |
| 질환 | cutaneous malignancies
|
scispacy | 1 | ||
| 질환 | cutaneous lesions
|
C5393824
Cutaneous lesions
|
scispacy | 1 | |
| 질환 | Anderson Cancer
|
scispacy | 1 | ||
| 질환 | Basal cell carcinoma
|
C0007117
Basal cell carcinoma
|
scispacy | 1 | |
| 질환 | squamous cell carcinoma
|
C0007137
Squamous cell carcinoma
|
scispacy | 1 | |
| 질환 | melanoma
|
C0025202
melanoma
|
scispacy | 1 | |
| 질환 | basal cell carcinomas
|
C4721806
Skin Basal Cell Carcinoma
|
scispacy | 1 | |
| 질환 | squamous cell carcinomas
|
C0007137
Squamous cell carcinoma
|
scispacy | 1 | |
| 질환 | melanomas
|
C0025202
melanoma
|
scispacy | 1 | |
| 질환 | nasal malignancies
|
scispacy | 1 | ||
| 기타 | nasal
|
scispacy | 1 | ||
| 기타 | men
|
scispacy | 1 | ||
| 기타 | women
|
scispacy | 1 |
MeSH Terms
Adolescent; Adult; Aged; Aged, 80 and over; Basal Cell Carcinoma; Carcinoma, Squamous Cell; Disease-Free Survival; Evaluation Studies as Topic; Female; Humans; Male; Melanoma; Middle Aged; Neoplasm Recurrence, Local; Nose; Prognosis; Retrospective Studies; Risk Factors; Skin Neoplasms; Surgery, Plastic; Surgical Flaps; Survival Rate
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