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Histopathological follow-up after bailout stenting for early postoperative stenosis of a central aorto-pulmonary shunt

Published online by Cambridge University Press:  18 April 2005

Matthias Peuster
Affiliation:
Department of Pediatric Cardiology and Pediatric Intensive Care, Georg-August University, Goettingen, Germany
Peter Wohlsein
Affiliation:
Department of Pathology, School of Veterinary Medicine Hannover, Hannover, Germany
Christian von Schnakenburg
Affiliation:
Department of Pediatric Cardiology and Pediatric Intensive Care, Georg-August University, Goettingen, Germany
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Abstract

We treated a neonate with pulmonary atresia and a ventricular septal defect complicated by straddling of the atrioventricular valves by constructing a central aorto-pulmonary shunt. The postoperative course was complicated by obstruction of the shunt, which was treated by implantation of a coronary stent. Six months after the stenting, a Glenn anastomosis was created and the stented shunt removed. Analysis showed that the shunt was completely covered by a vascularized neointima. The stent had not produced injury to the shunt, with struts of the stent covered nicely by neoendothelium, with sparse inflammation surrounding the artificial implants.

Information

Type
Brief Report
Copyright
© 2003 Cambridge University Press
Figure 0

Macroscopic view (a) of the stented polytetrafluoroethylene shunt removed at surgery. The struts (b) are incorporated into loosely arranged and endothelialized neointima supported by the polyteterafluoroethylene shunt; Richardson stain, original magnification 5 ×. There is neointimal tissue (c) close to a strut with loosely connected collagenous fibers. The shunt itself, however, reveals no destructive changes. Richardson stain, original magnification 40 ×. The luminal surface of the shunt (d) is composed of loosely arranged vascularized (→) connective tissue, Richardson stain, original magnification 40 ×.

Figure 1

Moderate granulomatous inflammation along the luminal surface of the shunt attached to the neointima (a) consists of macrophages and polynuclear giant cells (→); Hematoxylin–Eosin stain, original magnification 20 ×. The mild granulomatous infiltration along the outer surface of the shunt (b) consists of single macrophages and multinucleated giant cells (→). The polytetrafluoroethylene shunt itself displays irregular slit-like spaces. Hematoxylin–Eosin stain, original magnification 40 ×.