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1.
Liver Transpl ; 25(6): 934-945, 2019 06.
Artículo en Inglés | MEDLINE | ID: mdl-30882994

RESUMEN

Splenic artery (SA) ligation can be performed during liver transplantation (LT) to avoid portal hyperperfusion, which is involved in the pathogenesis of both small-for-size and SA syndrome. The SA can also be used as an inflow for arterial reconstruction. Exceptionally, SA interruption or agenesis has been associated with positive remodeling of collateral arteries supplying the spleen via the left gastric artery (LGA), short gastric vessels, and the gastroepiploic arcade (GEA), with subsequent severe upper gastrointestinal (GI) bleeding. To determine incidence, magnitude, predictors, and clinical implications of vascular remodeling after SA interruption during LT, we identified 465 patients transplanted in the period 2007-2017 who had the SA ligated or interrupted at LT. Among them, 88 had a computed tomography angiography suitable for evaluation of vascular remodeling after LT. The presence of prominent gastric arterial collaterals and the increase in LGA and GEA diameter were evaluated on 2-dimensional axial images and multiplanar reconstructions. Of the 88 patients, 28 (31.8%), 32 (36.4%), and 22 (25.0%) developed gastric collateralization graded as mild, moderate, or severe. Of the patients for whom comparison with pre-LT imaging was possible (n = 54), 51 (94.4%) presented a median 37% and 55% increase in LGA and GEA diameter, respectively. Severe gastric collateralization was associated with lower body mass index (odds ratio, 0.84; 95% confidence interval [CI], 0.71-0.98; P = 0.03), whereas a GEA caliper measurement increase was positively correlated with Model for End-Stage Liver Disease score (r2 = 0.12; 95% CI, 0.65-4.15; P = 0.008). Out of 465 patients, 2 (0.43%) had severe episodes of arterial upper GI bleeding, possibly exacerbated by vascular remodeling. In conclusion, vascular remodeling after SA interruption during LT is frequent and can aggravate GI bleeding during follow-up.


Asunto(s)
Enfermedad Hepática en Estado Terminal/cirugía , Hemorragia Gastrointestinal/epidemiología , Trasplante de Hígado/efectos adversos , Hemorragia Posoperatoria/epidemiología , Remodelación Vascular/fisiología , Circulación Colateral/fisiología , Angiografía por Tomografía Computarizada , Enfermedad Hepática en Estado Terminal/diagnóstico , Femenino , Estudios de Seguimiento , Artería Gástrica/diagnóstico por imagen , Hemorragia Gastrointestinal/etiología , Hemorragia Gastrointestinal/fisiopatología , Humanos , Hipertensión Portal/etiología , Hipertensión Portal/prevención & control , Ligadura/efectos adversos , Trasplante de Hígado/métodos , Masculino , Persona de Mediana Edad , Hemorragia Posoperatoria/etiología , Hemorragia Posoperatoria/fisiopatología , Índice de Severidad de la Enfermedad , Bazo/irrigación sanguínea , Arteria Esplénica/diagnóstico por imagen , Arteria Esplénica/cirugía , Resultado del Tratamiento
2.
Br J Radiol ; 97(1155): 505-512, 2024 Feb 28.
Artículo en Inglés | MEDLINE | ID: mdl-38419148

RESUMEN

Acellular dermal matrices (ADMs) are biological engineered tissues, which may provide an immunologically inert scaffold in breast reconstruction. Since the literature on imaging features of ADMs is limited, radiologists must be aware of the common imaging appearances of ADM, to differentiate normal conformation from residual or recurrent disease. Our purpose is to review the current role of ADMs in implant-based breast reconstruction, describing the normal imaging findings at ultrasound, mammography, and MRI also considering the possible changes over time. In this pictorial essay, we reviewed imaging features of ADMs described in the literature and we reported our experience in patients who underwent reconstructive surgery with human or animal ADM for newly diagnosed breast cancer.


Asunto(s)
Dermis Acelular , Neoplasias de la Mama , Mamoplastia , Cirugía Plástica , Animales , Humanos , Femenino , Mastectomía/métodos , Mamoplastia/métodos , Neoplasias de la Mama/diagnóstico por imagen , Neoplasias de la Mama/cirugía
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