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Published on: May 19, 2020
Tumorous deformity of mitral valve leaflet after chordal rupture in a child
Koichi Tamura1, Yuichi Sugisaki, Shunichi Ogawa
1Division of Surgical Pathology, Nippon Medical School Hospital, Tokyo, Japan. tamura@nms.ac.jp
Insights
A child developed a tumorous mitral valve deformity after chordal rupture. This overgrowth of valve tissue, driven by mitral regurgitation, may involve an imbalance of matrix metalloproteinases and tissue inhibitors.
Area of Science:
- Cardiovascular Pathology
- Pediatric Cardiology
- Surgical Pathology
Background:
- Spontaneous chordal rupture in the mitral valve can lead to regurgitation and leaflet complications.
- Tumorous deformities of heart valves are rare, particularly in pediatric cases.
Observation:
- A 9-year-old boy presented with a posterior mitral leaflet deformity following partial chordal rupture.
- Echocardiography revealed gradual development of tumorous bulging over 5 years.
- Histological analysis showed myxomatous material, mesenchymal cells expressing Vimentin, PCNA, MMP-1, MMP-2, and TIMP-1.
Findings:
- The tumorous mitral valve lesion consisted of myxomatous tissue with disorganized collagen and elastic fibers.
- Mesenchymal cells within the lesion exhibited high proliferation (PCNA index 29.3%) and expressed MMPs and TIMPs.
- An imbalance in matrix metalloproteinase (MMP) and tissue inhibitor of metalloproteinase (TIMP) activity was noted, particularly reduced TIMP-2 reactivity at the lesion surface.
Implications:
- Mitral regurgitation following chordal rupture can stimulate valve tissue overgrowth, leading to tumorous deformities.
- The imbalance between MMPs and TIMPs appears crucial in the pathogenesis of this mitral valve bulge formation.
- Understanding these molecular mechanisms may inform future therapeutic strategies for valvular heart disease in children.
Abstract:
A case with tumorous deformity of the posterior mitral valve leaflet after spontaneous chordal rupture in a child is described. A partial rupture in the chordae tendineae of the posterior mitral leaflet was found by echocardiography in a 9-year-old Japanese boy. Tumorous bulging was gradually developed in the leaflet and was surgically excised 5 years later. Multiple nodular tumors were found on the atrial surface of the posterior mitral leaflet. Histological examination revealed that the tumorous bulging consisted of myxomatous materials in which collagen fibrils and very fine elastic fibers were distributed loosely and irregularly. Normal-looking endothelial cells covered the luminal surface of the bulging lesion. Vimentin-positive spindle-shaped mesenchymal cells were scattered in the bulge area. The labeling index of proliferating cell nuclear antigen (PCNA) in these cells was 29.3%. These spindle cells were positive for matrix metalloproteinase (MMP)-1 in the entire bulge area. The cells and matrix were positive for MMP-2 and tissue inhibitor of MMP (TIMP)-1 in the basal area of bulging, but were weakly positive or negative at the surface area. Reactivity for TIMP-2 in the cells in the bulge area was obviously weaker than that in the cells at the spongiosa of the anterior mitral leaflet, which was obtained from the patient at the valve replacement operation 9 months after the initial operation. These findings indicated that the tumorous deformity of the mitral valve was formed by the overgrowth of valve tissue under the stimulation of mitral regurgitation in this child, and the imbalance of MMP and TIMP might play an important role in the bulge formation.
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