Literature DB >> 15083217

Lymphangiomas in infancy and childhood.

Ahmed H Al-Salem1.   

Abstract

OBJECTIVE: Lymphangiomas are rare congenital malformations, commonly seen in the head and neck. This is a review of our experience in the management of 22 children with lymphangiomas.
METHODS: The medical records of children with lymphangioma admitted to Qatif Central Hospital, Qatif, Kingdom of Saudi Arabia over a period of 10 years from August 1989 to July 2000 were retrospectively reviewed for age at diagnosis, gender, mode of presentation, site of lymphangioma, method of treatment and outcome.
RESULTS: We treated 22 children (12 females and 10 males) with lymphangioma. Their ages ranged from birth to 12 years, but majority (73%) were 4 years of age or younger. In 10 (45.5%), the lymphangioma involved the neck, 5 of them presented with sudden neck swelling as a result of hemorrhage into a lymphangioma, which caused diagnostic confusion. One patient had extensive lymphangioma involving the floor of the mouth, tongue, and left parotid gland. The remaining 11 patients had lymphangioma involving the parotid gland in 2, floor of the mouth in 3, and one each in the abdominal wall, above the right knee, mediastinum, breast, scrotum, and mesentery. All were treated surgically except 3 who were treated with intralesional bleomycin and showed complete disappearance of their lesions. There was recurrence in the child with mediastinal lymphangioma and a small recurrence in the child with bilateral lesions in the floor of the mouth.
CONCLUSION: Lymphangiomas are relatively rare, involving mainly the head and neck, but they can be rarely seen at other sites. An important observation is the sudden appearance of cervical lymphangioma as a result of hemorrhage, which should be kept in mind. Our experience in the treatment of lymphangiomas using bleomycin is limited to draw any conclusions. We therefore considered surgery as treatment of choice for lymphangiomas. However, sclerotherapy can be used when there is a risk of damaging surrounding structures, and also to obviate the poor cosmetic results.

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Year:  2004        PMID: 15083217

Source DB:  PubMed          Journal:  Saudi Med J        ISSN: 0379-5284            Impact factor:   1.484


  6 in total

1.  Single center experience with intralesional bleomycin sclerotherapy for lymphatic malformations.

Authors:  Hakan Yılmaz; Özlem Yılmaz; İlkay Çamlıdağ; Ümit Belet; Hüseyin Akan
Journal:  Jpn J Radiol       Date:  2017-08-04       Impact factor: 2.374

2.  Retroperitoneal and genital lymphangioma therapeutic challenges in a developing country.

Authors:  Jk Olabanji; Ao Oladele; Oc Famurewa; O Adejuyigbe; Sa Ademola
Journal:  Libyan J Med       Date:  2009-03-01       Impact factor: 1.657

3.  Lymphangiocele: A very rare cause of primary infertility.

Authors:  Sunita Samal; Sudeepta Kumar Swain; P Pallavee; Seetesh Ghose
Journal:  J Hum Reprod Sci       Date:  2015 Jan-Mar

4.  Infantile Cystic Hygroma: An Unusual Perioperative Course.

Authors:  Suman Saini; Madhu Dayal; Amita Gupta
Journal:  Anesth Essays Res       Date:  2017 Jan-Mar

5.  Pediatric breast lymphatic malformation with recurrent presentation in an adolescent female.

Authors:  Rachel Kaye; Rebecca Leddy
Journal:  BJR Case Rep       Date:  2021-09-10

6.  Intrathoracic cystic hygroma with sudden respiratory distress mimicking pneumonia.

Authors:  Umesh Goneppanavar; K N Prasad; Shwethapriya Rao; Souvik Chaudhury
Journal:  Indian J Crit Care Med       Date:  2012-07
  6 in total

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