Lymphangioma Circumscriptum Post Radiotherapy for Penile Cancer Treated with CO₂ Laser.

Acta Dermatovenerol Croat

Ancuta Proca Nicula, MD, PhD student, "Victor Babes" University of Medicine and Pharmacy, Dermatology Department, Eftimie Murgu No 2, 300041 Timisoara, Romania;

Published: April 2018

Lymphangioma circumscriptum (LC) is a rare, benign condition, predominantly characterized by the malformation of lymphatic skin vessels. Its onset may be congenital or due to secondary causes such as radiotherapy, infections, or surgical procedures. We present the case of a 55-year-old patient with a pathologic history of squamous cell carcinoma of the penis followed by radical penectomy. Due to metastasis to the locoregional lymph nodes, the entire affected area was subsequently treated with radiation therapy, receiving a total dose of 55.8 Gray. Eight years after this treatment, translucent vesicles filled with a clear liquid appeared on the scrotum. Histopathology confirmed the diagnosis of LC and therapy with CO2 laser was applied, resulting in a favorable outcome. LC of the scrotum may present a long-term radiotherapy-induced complication of this site. Our clinical experience showed that the CO2 laser was the therapy of choice as the vesicles entirely disappeared and healed as white scar-like lesions.

Download full-text PDF

Source

Publication Analysis

Top Keywords

lymphangioma circumscriptum
8
co2 laser
8
circumscriptum post
4
post radiotherapy
4
radiotherapy penile
4
penile cancer
4
cancer treated
4
treated co₂
4
co₂ laser
4
laser lymphangioma
4

Similar Publications

Lymphangioma circumscriptum, one of the common forms of lymphangioma, can be either congenital or acquired. Various acquired conditions can lead to its causation and one of the causes might be untreated hidradenitis suppurativa. So, this report highlights the need of early interventions for hidradenitis suppurativa as lymphangioma circumscriptum can be one of its consequences later in life.

View Article and Find Full Text PDF

Unlabelled: The RASopathies are a group of disorders resulting from a germline variant in the genes encoding the Ras/mitogen-activated protein kinase pathway. These disorders include Noonan syndrome (NS), cardiofaciocutaneous syndrome (CFC), Costello syndrome (CS), Legius syndrome (LS), and neurofibromatosis type 1 (NF1), and have overlapping clinical features due to RAS/MAPK dysfunction. In this study, we aimed to describe the clinical and molecular features of patients exhibiting phenotypic manifestations consistent with RASopathies.

View Article and Find Full Text PDF

Hamartomatous lymphatic channel proliferation causes lymphangiomas or microcystic lymphatic malformations (MLM). They are most commonly found in the head and neck, with oral occurrences a rarity. In this case, a 34-year-old woman presented with lymphangioma circumscriptum on the buccal mucosa, a condition that typically causes asymptomatic pebbly papules.

View Article and Find Full Text PDF
Article Synopsis
  • Lymphangioma is an abnormal growth of lymphatic vessels, with tongue lymphangiomas being relatively rare and traditionally associated with high recurrence rates after treatment.* -
  • This study presents two cases where coblation, a form of radiofrequency ablation, was used successfully on tongue lymphangiomas, resulting in rapid recovery and minimal pain for the patients.* -
  • The findings suggest that radiofrequency ablation leads to better healing and no recurrence after one year, making it a preferred treatment option for oral lymphangiomas.*
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!