http://www.casereports.in/articles/4/2/Spindle-Cell-Sarcoma-Arising-from-Nerve-Sheath-Presenting-as-Huge-Abdominal-Mass.html
Spindle Cell Sarcoma Arising from Nerve Sheath Presenting as Huge Abdominal Mass
| Sohail Shaikh, Rajshree Dayanand Katke, Soham Dilip Raut
From the Department of Surgery1 and Department of Obstetrics & Gynecology2, Grant Government Medical College & Sir J. J. Group of Hospitals, Mumbai, Maharashtra, India.
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Introduction
Spindle
cell sarcoma is a type of connective tissue cancer in which the cells
are spindle-shaped when examined on microscopy. The tumors generally
begin in nerve sheath, layers of connective tissue such as that under
the skin, between muscles, and surrounding organs, mesocolon, and will
generally start as a small lump with inflammation that grows. Spindle
cell tumors are low grade fibromyxoid soft tissue sarcoma and
microscopic appearance with features of both mesenchymal and
neuroendocrine differentiation. Cytogenetic studies of spindle cell
tumor show two cell lines containing balanced translocation between
chromosomes 7 and 16 [1].
A small group of both low grade fibromyxoid soft tissue sarcoma and
hyalinizing spindle tumor (HSCT) shows areas of increased cellularity
and atypia which are grouped as intermediate to high grade sarcoma [2]. A rare case of spindle cell carcinoma is documented in the esophagus [3]. These tumors rarely metastasize, but pulmonary metastases are documented [4,5].
Case Report
A
case of 65 year old female, housewife, presented through the outpatient
department with one month history of abdominal swelling and distention,
weight loss, intermittent constipation and dysuria. Her vitals were
within normal limits. On examination, abdomen was distended with everted
umbilicus, dilated veins on left lower quadrant of abdomen with a hard
non-tender mass almost occupying the whole of the abdomen arising from
pelvis reaching up to just 5 cm below xiphisternum with smooth surface.
Patient was previously operated for total abdominal hysterectomy with
bilateral salpingoophorectomy, seven years ago for ovarian cancer.
CT
scan report was suggestive of 19.5x16.3x13 cm well defined,
heterogeneously enhancing mass lesion with necrotic areas in the
midline arising from the pelvis and extending up to L3 vertebral body.
The mass was compressing the bladder though the fat planes were
maintained. The mass was reported most likely to be a neoplastic lesion
[Fig.1]. Midline exploratory laparotomy showed a jelly like mass in the
abdominal cavity and pelvis reaching up to the base of pelvis. The mass
was approximately 20x15 cm in size, smooth in surface and rounded in
shape [Fig.2]. Mass was separated from the surrounding structures and
excised. Weight of the mass was 4.5 kg, measured after the surgery.
Postoperative follow-up in the ward was uneventful and patient was
transfused for the compensating the blood loss of about 700 ml during
the surgery.
Histopathology
report was suggestive of high grade spindle cell sarcoma [Fig.3].
Several foci of tumor necrosis. nuclear pleomorphism and mitotic
activity were conspicuous. On immunohistochemistry, tumor cells were
positive for S-100 with negative Desmin and SMA. Thus possibility of
smooth cell differentiation was excluded and possibility of malignant
nerve sheath tumor favored. No ovarian parenchyma was recognized.
Patient was then referred to oncology for radiotherapy.
Discussion
Spindle
cell sarcoma is a type of connective tissue cancer in which the cells
are spindle-shaped when examined microscopically Spindle cell sarcoma is
a rare cause of large abdominal mass [6]. Cytological diagnosis of spindle cell tumor is difficult as compared to other soft tissue tumors [7].
These tumors generally begin in layers of connective tissue such as
that under the skin, between muscles, and surrounding organs, and will
generally start as a small lump that grows gradually. At first the lump
is self-contained as the tumor exists in earlier stages, and will not
necessarily expand beyond its encapsulated form. However, it may develop
malignant processes that can only be detected through microscopic
examination. As such, at this level the tumor is usually treated by
excision that includes wide margins through healthy-looking tissue,
followed by thorough biopsy and additional excision if necessary. In
high grade lesions, prognosis is grim and chemotherapy and radiation are
the only methods of controlling the cancer.
Spindle
cell sarcoma can develop for a variety of reasons, including genetic
predisposition but it also may be caused by a combination of other
factors including injury and inflammation in patients that are already
thought to be predisposed to such tumors. Spindle cells are a naturally
occurring part of the body’s response to injury. In response to an
injury, infection, or other immune response the connective tissues will
begin dividing to heal the affected area, and if the tissue is
predisposed to spindle cell cancer the high cellular turnover may result
in a few becoming cancerous and forming a tumor.
Spindle
cell tumors are usually diagnosed on histopathology based on picture
comprising of elongated spindle cells arranged in interlacing fascicles
and bundles with herring bone pattern at places. These bundles intersect
each other at wide angles at places showing storiform pattern with
eosinophilic cytoplasm and cigar shaped nuclei. Occasionally ghost cells
in the center and multinucleated giant cell may present, grading is
suggested in soft tissue sarcoma in order to improve the management,
prognosis and to prevent the recurrence, based on nuclear atypia,
nuclear overlap, mitotic figures, and necrosis these tumors are given
grades [8,9]. Treatment of spindle cell tumor is its complete excision [10].
Radiotherapy has minimal role and the tumor tends to recur. In our
case, spindle cell sarcoma of nerve sheath occurring in the abdomen was a
rare case. The size upto which it progressed posed a great challenge
during surgery as the tumor mass was jelly like and friable. The tumor
had to be meticulously dissected away from the small bowel at the same
time achieving adequate hemostasis.
References
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