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Extended Chest Wall Resection for Aggressive Fibromatosis of Breast. Reconstruction with Mesh Graft and TRAM Flap

Case Report | Open Access | Volume 3 | Issue 1

  • 1. Department of Surgery, Bács-Kiskun Teaching County Hospital, Hungary
  • 2. Department of Pathology, Bács-Kiskun Teaching County Hospital, Hungary
  • 3. Department of Cardiology, Bács-Kiskun Teaching County Hospital, Hungary
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Corresponding Authors
Károly Kovács, 6 Szép Ilonka str. 6000 Kecskemét, Hungary, Tel: 36-30-206-2166; Fax: +36-76-481-219
ABSTRACT

Desmoid tumours in the chest are rare borderline tumours. The primary treatment of a tumour is the radical surgical resection. We present the case of a 23-year-old woman who had surgical resection by right breast tumor. The CT examination showed infiltration of sternum margin and some ribs. We resected the tumour together with a half of the right breast and performed the partial resection of the sternum and four ribs. We reconstructed the chest wall by artificial mesh graft and right TRAM flap.

The patient did not receive oncological treatment. 6 years after the surgical treatment the patient is symptoms and recurrence free.

KEYWORDS

•    TRAM flap
•    Desmoid tumour

CITATION

Füstös L, Kovács K, Fekete L, Oláh C, Cserni G, et al. (2015) Extended Chest Wall Resection for Aggressive Fibromatosis of Breast. Reconstruction with Mesh Graft and TRAM Flap J Surg Transplant Sci 3(1): 1008.

ABBREVIATIONS

TRAM: Transverse Rectus Abdominis Myocutaneus

CASE PRESENTATION

We present the case of a 23-year-old woman who had surgical resection by right breast tumour, after fine needle aspiration cytology and mammography examinations. The pathological report showed aggressive fibromatosis of the breast. Half a year later we detected a local recurrence of the tumour. At this time the CT examination showed infiltration of the sternum margin and four ribs (Figure 1).

CT image before the operation.

Figure 1: CT image before the operation.

The tumour expanded during her second pregnancy (Figure 2).

Photo of the patient before the operation.

Figure 2: Photo of the patient before the operation.

We were able to perform the final surgical treatment two and a half years after the detection of the local recurrence of the tumour (Figure 3).

The plastic surgical plan of the operation.

Figure 3: The plastic surgical plan of the operation.

The operation strategy was planned with the cooperation of a plastic surgeon. The chest wall affected by the tumour is shown in (Figure 4) [1,2].

The chest wall area affected by the tumour.

Figure 4: The chest wall area affected by the tumour.

The tumour was resected together with a half of the right breast. The partial resection of the sternum and four ribs was performed. In order to supplement the chest wall, a mesh graft was implanted and the soft tissue was recovered by a TRAM flap (Figure 5).

Reconstruction of the chest wall by mesh graft.

Figure 5: Reconstruction of the chest wall by mesh graft.

Intraoperative pathological examination ensured that the resection margin was tumour free. We reconstructed the chest wall by artificial mesh graft and right TRAM flap (Figure 6).

Photo of the patient after surgery.

Figure 6: Photo of the patient after surgery.

The histological report showed that the  tumor consisted of cytologically bland spindle cells entrapping lobules, ducts and nerves and infiltrating skeletal muscle fibers of the major pectoral muscle. The tumor cells were immunoreactive for smooth muscle actin and were negative for cytokeratins (AE1/AE3, 34Beta-E12), p63, desmin, CD34, S100. The proliferation rate as assessed by the Ki-67 labeling index was <1%. This phenotype is in keeping with the diagnosis of fibromatosis. (No Beta-catenin staining was available at the time of diagnosis) (Figure 7) [3-6].

Histological image of the tumour /haematoxylin and eosin  x400/.

Figure 7: Histological image of the tumour /haematoxylin and eosin x400/.

The patient recovered without any complications (Figure 8).

Photo of the patient 4 weeks after the operation.

Figure 8: Photo of the patient 4 weeks after the operation.

During the follow-up no recurrence was detected (Figure 9). 6 years after the operation the patient’s 4th child was born.

CT image of the chest 4 years after the operation

Figure 9: CT image of the chest 4 years after the operation

DISCUSSION

Fibromatosis is rare among primary breast tumours. This is a non-malignant disease of the breast [7,8]. After successful surgical treatment the local recurrence is up to 25% of the cases. At an advanced stage fibromatosis can infiltrate the chest wall.

In neglected cases, the resection of the soft tissue and the chest wall can be a big challenge. After the RO resection plastic surgical methods are often necessary for the reconstruction [9]. Usually no oncological treatment is necessary after the operation [10]. Close follow-up of the patient and optional repeated operation can be a way of treatment.

REFERENCES

1. Salemis NS, Nakos G, Tsiambas E, Tsantilas V, Seretis C. Rapidly growing myofibroblastoma of the breast diagnosed in a premenopausal woman: management and review of the literature. Breast Dis. 2012; 34: 29-34.

2. Mele M, Jensen V, Wronecki A, Lelkaitis G. Myofibroblastoma of the breast: Case report and literature review. Int J Surg Case Rep. 2011; 2: 93-96.

3. Powari M, Srinivasan R, Radotra BD. Myofibroblastoma of the male breast: a diagnostic problem on fine-needle aspiration cytology. Diagn Cytopathol. 2002; 26: 290-293.

4. Magro G. Mammary myofibroblastoma: a tumor with a wide morphologic spectrum. Arch Pathol Lab Med. 2008; 132: 1813-1820.

5. Shivali B, Kataria S, Chandramouleeswari K, Anita S. Myofibroblastoma Breast with Unusual Morphological Features. Cytohistopathological Diagnostic Pitfalls And Role Of Immunohistochemistry - Review Of Literature. J Clin Diagn Res. 2013; 7:2323-2325.

6. Qureshi A, Kayani N. Myofibroblastoma of breast. Indian J Pathol Microbiol. 2008; 51: 395-396.

7. Abeysekara AM, Siriwardana HP, Abbas KF, Tanner P, Ojo AA. An unusually large myofibroblastoma in a male breast: a case report. J Med Case Rep. 2008; 2: 157.

8. Lee YS, Gilcrease M, Wu Y, Yang WT. Myofibroblastoma of the breast: Imaging features. Eur J Radiol Extra. 2009; 73: 13-15.

9. Shah SN. Giant myofibroblastoma of breast: a case report. Indian J Pathol Microbiol. 2007; 50: 583-585.

10. Das P, Sharma A, Arora R, Singh MK. Myofibroblastoma of breast. Indian Journal of Med Paediatr Oncol. 2008; 29: 16-19.

Füstös L, Kovács K, Fekete L, Oláh C, Cserni G, et al. (2015) Extended Chest Wall Resection for Aggressive Fibromatosis of Breast. Reconstruction with Mesh Graft and TRAM Flap J Surg Transplant Sci 3(1): 1008.

Received : 15 Jan 2015
Accepted : 15 Feb 2015
Published : 16 Feb 2015
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