- Case report
- Open Access
Surgical excision of an abdominal wall granular cell tumour with Permacol®mesh reconstruction: a case report
© Chaudhry et al; licensee BioMed Central Ltd. 2008
- Received: 04 January 2008
- Accepted: 25 February 2008
- Published: 25 February 2008
Granular cell tumours of the abdominal wall are extremely rare: less than 10 have been reported in the worldwide medical literature. We report this interesting case, review the relevant literature on this tumour and discuss surgical abdominal wall reconstruction options.
A 70 year old lady presented with a left abdominal mass. This was thought to be a soft tissue sarcoma on CT imaging prior to surgical excision. En-bloc surgical resection was performed. Surgical reconstruction of the abdominal wall defect was performed using Permacol® mesh. Histopathological examination of the surgical specimen showed it to be a granular cell tumour.
Although rare, granular cell tumours can present as an abdominal wall mass. It is important that clinicians are aware of their existence. The closure of large defects, after surgical resection of abdominal wall tumours, is a surgical challenge. We used a new biosynthetic procine mesh (Permacol®) which appeared to work well in this situation.
- Abdominal Wall
- Abdominal Wall Defect
- Granular Cell Tumour
- Transversus Abdominis
- Abdominal Wall Reconstruction
Granular cell tumours (GCT) are rare neural tumours characterized by large granular appearing eosinophilic cells. GCTs were initially considered to be of striated muscle origin by Abrikossoff who described a tumour arising from the tongue in 1926 . Older terms for this tumour type include granular cell myoblastoma, granular cell neuroma, granular cell neurofibroma and granular cell schwannoma. However, newer investigational techniques such as electron microscopy and immunnohistochemistry have proven that GCTs are most likely derived from Schwannoma cells of the peripheral nerve fibres [2, 3]. Most GCTs are benign, but rare malignant types have been reported. The tongue is the single most common anatomical site, but GCTs can be found in virtually any body site, including skin, subcutaneous tissue, breast, rectum, oesophagus and vulva . Previously only seven cases of abdominal wall GCTs have been reported in the medical literature .
We describe a new case of a GCT arising from the abdominal wall muscles in a 70 year old lady. We briefly review the medical literature on this tumour and discuss the surgical abdominal wall reconstruction options pertinent to this case.
A 70 year old lady was referred urgently to the colorectal clinic with a palpable abdominal mass. She presented to her General Practitioner (GP) with left sided abdominal pain, diarrhoea and weight loss. Her GP found a suspicious left sided abdominal mass on examination and referred her urgently under the two week colorectal cancer rule. Her past medical history included hypertension, chronic obstructive airways disease and appendicectomy. She also had a previous total abdominal hysterectomy and bilateral salpingo-oopherectomy for large uterine fibroids.
This patient has been reviewed in the outpatient clinic and is currently alive and well five months after surgery.
GCTs typically present as a small, poorly circumscribed, painless, non-ulcerating nodule. The tumours can arise from virtually any anatomical site; the most common sites are the head and neck (especially tongue), the chest wall and the arm. They are mainly located in the dermis or the subcutaneous tissue (66% of cases) and less frequently submucosa, smooth muscle or striated muscle. They also can arise in the internal organs: larynx, bronchus, stomach, anogenital region and bile ducts. They are mainly solitary, although they can be multiple (10–15%). They can occur at any age, but are most common in the fourth, fifth and sixth decades of life and are rare in children . Females tend to be affected twice as frequently as males.
The histopathological differential diagnosis can include rhabdomyoma (contains cross-striations and glycogen); hibernoma and fibroxanthoma (contain lipid droplets); and reactive changes with surgical trauma (associated with inflammatory elements and areas of necrosis). A common site for a rhabdomyoma is the heart, which is helpful in the differential diagnosis. GCTs can also be mistaken for squamous cell carcinoma due to marked acanthosis and pseudoepitheliomatous hyperplasia. Immunohistochemistry is essential for the correct diagnosis . Most GCTs stain positive for S100, neuron-specific enolase, NK1-C3 and CD68. They stain negative for epithelial, endothelial and smooth muscle markers.
Patients with completely resected benign lesions are usually cured. Excluding malignant tumours, recurrence is rare (it is more common if complete surgical excision is not achieved). Therefore the prognosis for these tumours appears to be favourable. There is no role for adjuvant therapy with radiotherapy or chemotherapy.
Malignant GCTs are encountered in only 2% of cases . Only around 80 cases have been reported worldwide. They are characterised by necrosis, spindling, vesicular nuclei with prominent nucleoli, increased mitotic activity (> 2 mitoses/10 high power fields), a high nuclear to cytoplasmic ratio and pleomorphism. More than 3 of these features are required for a diagnosis of malignancy. Less than 3 of these features would classify the tumour as an atypical GCT. The prognosis of malignant GCT is poor with risk of local recurrence and distant metastases to lung, liver and bone. Interestingly, four of the reported seven GCTs of the abdominal wall have had malignant features. Our case showed the typical histopathological features of a GCT with no suspicious features of malignancy. However, given the high percentage of malignant lesions reported to be arising from the abdominal wall careful histopathological examination of this anatomical site is recommended.
Extensive abdominal wall defects like the one encountered here are a surgical challenge . The options for surgical closure included: primary closure, the use of prosthetic mesh material and advanced plastic surgical techniques . Primary closure has a high risk of future incisional hernia formation. Plastic surgical techniques (such as pedicled or free myocutaneous flaps from various sites including the rectus abdominis, latissumus dorsi or gracilis muscles) require advanced plastic surgical training and expertise.
The ideal material for the repair of abdominal wall defects would provide strength, flexibility, host tissue incorporation, and infection resistance. There is a wide variety of mesh material available for abdominal wall reconstruction . Complications associated with the use of permanent synthetic biomaterials (such as prolene mesh) include foreign body reaction, small bowel obstruction, intestinal fistulation, erosion of the mesh material into adjacent abdominal viscera, and mesh shrinkage or migration . These risks are particularly high when permanent mesh is placed in direct contact with the bowel and abdominal viscera. However, the newer biosynthetic material meshes, such as Permacol (manufactured from porcine collagen) or Alloderm (manufactured from human cadaveric collagen), do not appear to be at risk of this problem . Permacol mesh is manufactured from acellular porcine collagen and is non-allergenic . Its principal benefits include less adhesion formation, good incorporation into host tissue and resistance to infection. It does not elicit a foreign body response and is readily colonised by host tissue cells and blood vessels thus making it resistant to infection. It is soft and flexible yet has high tensile strength and is available in various sizes, making it ideal for closing abdominal wall defects. It has potential uses in complex incisional hernia repair, para-stomal hernia repair, abdominal wall reconstruction and cosmetic surgery.
Although rare, GCTs can present as an abdominal wall mass. It is important that clinicians are aware of their existence. The closure of large defects, after surgical resection of abdominal wall tumours, is a surgical challenge. We used a new biosynthetic porcine mesh (Permacol®) to close the large abdominal wall defect and this appeared to be ideal for this particular situation.
Written informed consent was obtained from the patient for publication of this Case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
The authors thank the patient for allowing this case to be published and the Medical Photography team for taking the clinical photographs.
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