| Literature DB >> 32792877 |
Magdalena Raszewska-Famielec1,2, Adam Borzêcki1, Dorota Krasowska3, Grażyna Chodorowska3.
Abstract
INTRODUCTION: To date, there has been no consensus either on the method, frequency or total duration of follow-up for patients that have developed a basal cell carcinoma (BCC). AIM: To evaluate usefulness of high-frequency ultrasound in monitoring patients with BCC, particularly to detect residual disease or early recurrence.Entities:
Keywords: basal cell carcinoma; dermatoscopy; high-frequency ultrasonography; monitoring of basal cell carcinoma
Year: 2020 PMID: 32792877 PMCID: PMC7394171 DOI: 10.5114/ada.2020.96099
Source DB: PubMed Journal: Postepy Dermatol Alergol ISSN: 1642-395X Impact factor: 1.837
Figure 1A – Dermatoscopy of basal cell carcinoma (BCC) of the nasal region. B – Ultrasonic image shows hypoechogenic, homogenous, well-defined structure. C – Dermatoscopy of the scar 4 weeks after surgery – in histology examination of the margin presence of cancer tissue. D – Ultrasonic image shows no evidence of cancer formation. E – Dermatoscopy of the scar 24 weeks after surgery shows multiple telangiectasia. F – Ultrasonic image 24 weeks after surgery shows no evidence of cancer formation
Figure 2A – Nodular basal cell carcinoma (nBCC) of the temporal region. B – Ultrasonic image shows hypoechogenic, heterogeneous oval structure. C – Dermatoscopy of the scar 4 weeks after surgery – in histology examination, the clear surgical margin < 0.2 cm. D – Ultrasonic image 4 weeks after surgery shows hypoechogenic, not well defined structure. E – Dermatoscopy 12 weeks after surgery shows multiple telangiectasia inside the scar. F – Ultrasonic image 12 weeks after surgery reveals reduction in hypoechogenic, not well defined structure. G – Dermatoscopy 24 weeks after surgery shows telangiectasia surrounding the scar. H – Ultrasonic image 24 weeks after surgery shows no evidence of residual disease
Figure 3A – Nodular, ulcerated basal cell carcinoma of the temporal region. B – Ultrasonic image shows hypoechogenic, heterogeneous bean like structure. C – Dermatoscopy of the scar 4 weeks after surgery – in histology, the clear surgical margin. D – Ultrasonic image 4 weeks after surgery shows hypoechogenic, quite well-defined, spindle structure. E – Dermatoscopy of the scar 12 weeks after surgery shows no clear evidence of residual disease. F – Ultrasonic image 12 weeks after surgery shows enlargement of hypoechogenic, well-defined spindle structure. Biopsy confirmed residual disease
Residual disease after treatment in examined basal cell carcinoma
| BCC type | Treatment method | Histopathological examination | Ultrasonographic examination | Residual disease (verified by histopathological examination) |
|---|---|---|---|---|
| Nodular BCC ( | SurgicalRemoval ( | Presence of cancer cells in surgical margin ( | Hypo- or heteroechogenic irregularly shaped focal echo enlarging on subsequent visits ( | Residual disease ( |
| No signs of residual disease ( | No signs of residual/recurrent disease was observed during 24 months of follow-up ( | |||
| Margin of surgical removal < 0.2 cm ( | No signs of residual disease ( | No signs of residual/recurrent disease was observed during 24 months of follow-up ( | ||
| Hypo- or heteroechogenic irregularly shaped focal echo normalizing on subsequent visits ( | ||||
| Margin of surgical removal > 0.2 cm ( | No signs of residual disease ( | No signs of residual/recurrent disease was observed during 24 months of follow-up ( | ||
| Superficial BCC ( | Surgical removal ( | Margin of surgical removal > 0.2 cm ( | No signs of residual disease ( | No signs of residual/recurrent disease was observed during 24 months of follow-up ( |
| ALA-PDT ( | Confirmation of sBCC ( | No signs of residual disease ( | No signs of residual/recurrent disease was observed during 24 months of follow up ( | |
| Linear hypoechogenic area ( | Residual disease ( | |||
| Micronodular BCC ( | Surgical removal | Margin of surgical removal > 0.2 cm ( | No signs of residual disease ( | No signs of residual/recurrent disease was observed during 24 months of follow-up ( |
| Morpheiform BCC ( | ||||
| Mixed BCC ( |