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Archivos de Investigación Materno Infantil

ISSN 2007-3194 (Print)
Órgano de difusión oficial del Instituto Materno Infantil del Estado de México
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2013, Number 3

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Arch Inv Mat Inf 2013; 5 (3)

Planeación terapéutica en un hemangiolinfangioma gigante toracoabdominal

Pérez LH, Cisneros GLC, Barba RE
Full text How to cite this article

Language: Spanish
References: 6
Page: 113-117
PDF size: 159.89 Kb.


Key words:

Hemangiolymphangioma, strategy multidisciplinary.

ABSTRACT

Introduction: Hemangiolymphangiomas are congenital malformations of the lymphatic and vascular system. The clinical symptom is a tumor that causes esthetic and functional troubles. The management of the patients can include monitor symptoms, sclerosing therapy and the extirpation or reduction of the volume of the tumor. The objective of this article is to state the strategic plan of giant toracoabdominal hemangiolymphangioma management in children. Clinical case: Two year old, male with giant toracoabdominal hemangiolymphangioma, prenatal detection confirmed at birth. With the preoperative projection of 100% of total body weight of patient. To admission the patient weight 27 kg, a tumor since the axilary fossa to the inguinal area and showed a collateral tumor over the left shoulder and the side face of thorax. A multidisciplinary team decided a two steps resection. The first surgery consisted of placement of venous access, invasive monitoring. a long incision and the nutrient vessels were ligated, the tumor was removed in a block, after that it was placed a drainer and the flaps were rotated. Findings tumor 15 kg, the evolution of the patient was satisfactory. Two months after, shows an increase of the left axilar lesion, so we decided to performing the surgery under the same lines that the previous. Findings: tumor of 785 g. Six months after the patient hasn’t showed signs of relapse. Discussion: Toracoabdominal hemangiolymphangioma in Childs is rare, the giant lesions and systemic troubles, requires an accurate surgical management. The case presented before was the result of a carefully planned and multidisciplinary strategy.


REFERENCES

  1. Okazaki T, Iwatani S, Yanai T, Kobayashi H, Kato Y, Marusasa T et al. Treatment of lymphangioma in children: our experience of 128 cases, J Pediatr Surg, 2007; 42: 386-389.

  2. Singh O, Singh GS, Upadhyaya VD, Sharma SS, Lahoti BK, Mathur RK. Cystic lymphangioma of the breast in a 6-year-old boy, J Pediat Surg, 2009; 44: 2015-2018.

  3. Alqahtani A, Nguyen LT, Flageole H, Shaw K, Laberge JM. 25 years’ experience with lymphangiomas in children, J Pediatr Surg, 1999; 34: 1164-1168.

  4. Gimeno AM, Colomar PP, González MI, Ollero CJM. Aspectos clínicos y morfológicos de los linfangiomas infantiles: revisión de 145 casos, An Esp Pediatr, 1996; 45: 25-28.

  5. Luzzatto C, Midrio P, Tchaprassian Z, Guglielmi M. Sclerosing treatment of lymphangiomas with OK-432, Arch Dis Child, 2000; 82: 316-318.

  6. Mata C, Larrache J, Alzina V. Linfangioma de pared torácica. A propósito de un caso, Rev Med Univ Navarra, 2002; 46: 38-40.




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Arch Inv Mat Inf. 2013;5