Yu-Ching Feng1, Kuan-Sheng Chen, Shih-Chieh Chang. 1. Veterinary Medical Teaching Hospital, College of Veterinary Medicine, National Chung Hsing University, 250 Kuo-Kuang Road, Taichung 40227, Taiwan.
Abstract
This animal was presented with a large-sized infiltrative lipoma in the abdominal wall that had been noted for 4 years. This lipoma was confirmed by histological examination from a previous biopsy, and the infiltrative features were identified by a computerized tomography scan. The surgical removal created a large-sized abdominal defect that was closed by a combination of latissimus dorsi and external abdominal oblique muscle flaps in a pedicle pattern. A small dehiscence at the most distal end of the muscle flap resulted in a small-sized abdominal hernia and was repaired with cranial sartorius muscle flap 14 days after surgery. The dog was in good general health with no signs of tumor recurrence after 18 months of follow-up.
This animal was presented with a large-sized infiltrative lipoma in the abdominal wall that had been noted for 4 years. This lipoma was confirmed by histological examination from a previous biopsy, and the infiltrative features were identified by a computerized tomography scan. The surgical removal created a large-sized abdominal defect that was closed by a combination of latissimus dorsi and external abdominal oblique muscle flaps in a pedicle pattern. A small dehiscence at the most distal end of the muscle flap resulted in a small-sized abdominal hernia and was repaired with cranial sartorius muscle flap 14 days after surgery. The dog was in good general health with no signs of tumor recurrence after 18 months of follow-up.
An 8-year-old, intact male, mixed breed dog was presented with intermittent hematuria and a
mass in the right inguinal region for 4 years (Fig.
1A). Concurrently, calculi in the urinary bladder were seen by radiographic examination
(Fig. 1B). Subsequently, two large stones were
removed by cystotomy, and incisional biopsy of the abdominal mass was performed for histologic
examination. Histopathologic diagnosis was lipoma. However, based on the history and anatomic
site of this mass, diagnosis of a suspected lipoma with infiltration to abdominal wall
musculature was made. Subsequently, the patient was referred to the Veterinary Medical
Teaching Hospital, National Chung Hsing University for further evaluation. On presentation,
the dog was bright, alert and responsive with normal vital parameters. A large-sized
subcutaneous mass in the right inguinal region was found. It was firm on palpation, with
ill-defined demarcation and was firmly fixed with the underlying abdominal wall. This mass
measured 15.1 × 8.5 × 5.5 cm in size. Palpation of peripheral lymph nodes displayed
unremarkable findings. A complete blood count and serum biochemistry were performed, and the
results were within normal reference limits. A computerized tomography (CT) scan (Alexion,
Toshiba Medical Systems Corporation, Otawara, Japan) was scheduled to further assess the
extent and margins of this mass, and for surgical planning.
Fig. 1.
Gross appearance of the mass located in the right inguinal region and the associated
images by radiography and computerized tomography (CT) scan. A, The mass was located on
the right inguinal region. B, Ventrodorsal view of abdominal radiograph. A mass of fat
opacity in the right inguinal region and cystolithiasis were seen by radiographic
examination. The urinary bladder was displaced to the left by the mass. C and D, The
mass was hypoattenuating with a mean hounsfield unit of −130. The mass had infiltrated
through the musculature of the abdominal wall. The muscles were fragmented with a
mottled appearance. Contrast images revealed that two arteries (the right cranial
abdominal and deep circumflex arteries) supplied the mass, but the mass did not show an
enhanced contrast. The urinary bladder was displaced to the left by the mass.
Gross appearance of the mass located in the right inguinal region and the associated
images by radiography and computerized tomography (CT) scan. A, The mass was located on
the right inguinal region. B, Ventrodorsal view of abdominal radiograph. A mass of fat
opacity in the right inguinal region and cystolithiasis were seen by radiographic
examination. The urinary bladder was displaced to the left by the mass. C and D, The
mass was hypoattenuating with a mean hounsfield unit of −130. The mass had infiltrated
through the musculature of the abdominal wall. The muscles were fragmented with a
mottled appearance. Contrast images revealed that two arteries (the right cranial
abdominal and deep circumflex arteries) supplied the mass, but the mass did not show an
enhanced contrast. The urinary bladder was displaced to the left by the mass.The dog was premedicated with dexmedetomidine (65 µg/m2, IV) and
midazolam (0.2 mg/kg, IV) and induced with propofol (1 mg/kg, IV). Anesthesia was maintained
with isoflurane after intubation. The dog was placed in sternal recumbency. A CT scan was
performed from the level of T8 to the hip joint. Following the plain CT scan, 2
ml/kg of contrast medium (Optiray, GE Healthcare, Cork, Ireland) was
administered, and the CT scan was repeated. The CT scan revealed that there was a homogeneous
hypoattenuating mass approximately 15.4 × 12.7 × 9.1 cm in the right inguinal region with a
mean hounsfield unit of −130 which was compatible with normal subcutaneous fat tissue. The mass
had infiltrated to the musculature of the abdominal wall, including the external abdominal
oblique, internal abdominal oblique, transversus abdominis and rectus abdominis muscles. The
muscles were fragmented with a mottle appearance. Contrast images revealed that two arteries
(right cranial abdominal and deep circumflex arteries) supplied the mass, but the mass did not
show an enhanced contrast. The urinary bladder was displaced to the left by the mass
(Fig. 1C and 1D).Ten days after the CT examination, surgical removal of this infiltrative lipoma of the
abdominal wall was performed with 1- to 2-cm margins. The dog was premedicated with
dexmedetomidine (125 µg/m2, IV) and midazolam (0.2 mg/kg, IV) and
induced with propofol (1 mg/kg, IV). An endotracheal tube was placed. Anesthesia was
maintained with isoflurane. The dog was placed in left lateral recumbency. An “L-shaped” skin
incision was made. A caudal incision line was conducted from the cranial border of the iliac
wing to the inguinal region, and a lateral incision was made from the inguinal region to the
9th rib. Skin and subcutaneous adipose tissues were bluntly dissected till exposure of the
external abdominal oblique muscle was achieved. A large mass beneath this muscle was seen. The
external abdominal oblique, internal abdominal oblique, rectus abdominis and transversus
abdominis muscles were severed with 1–2 cm surgical margins of normal tissues. Resection of
the abdominal wall was performed with a bipolar vessel sealing device (LigaSure small jaw
instrument, Covidien, Plymouth, MN, U.S.A.) and a monopolar electrocautery while carefully
distinguishing normal fat from the tumor. Visceral organs were exposed after mass removal
(Fig. 2A).
Fig. 2.
Closure of the large-sized abdominal defect with muscle flaps. A, The musculatures of
the abdominal wall were severed with 1–2 cm surgical margins of normal tissues and
removed with the mass. A large abdominal defect was created, and visceral organs were
exposed after mass removal. B, The lateral skin incision was further extended cranially.
The latissimus dorsi muscle (white asterisk) was resected at the level of the 6th rib
cranially and below the transverse process of the spine dorsally. The cranial portion of
the external abdominal oblique muscle (white triangle) was severed from its rib
attachment. Both muscles were undermined, elevated till their attachment to the 11th rib
and reversed 180 degrees to completely cover the large defect. C, The latissimus dorsi
(white asterisk) and external abdominal oblique muscle (white triangle) flaps were
sutured with the residual abdominal wall and hypaxial muscle with 2–0 polydioxanone,
simple interrupted pattern.
Closure of the large-sized abdominal defect with muscle flaps. A, The musculatures of
the abdominal wall were severed with 1–2 cm surgical margins of normal tissues and
removed with the mass. A large abdominal defect was created, and visceral organs were
exposed after mass removal. B, The lateral skin incision was further extended cranially.
The latissimus dorsi muscle (white asterisk) was resected at the level of the 6th rib
cranially and below the transverse process of the spine dorsally. The cranial portion of
the external abdominal oblique muscle (white triangle) was severed from its rib
attachment. Both muscles were undermined, elevated till their attachment to the 11th rib
and reversed 180 degrees to completely cover the large defect. C, The latissimus dorsi
(white asterisk) and external abdominal oblique muscle (white triangle) flaps were
sutured with the residual abdominal wall and hypaxial muscle with 2–0 polydioxanone,
simple interrupted pattern.The lateral skin incision was further extended to the level of the 4th rib. Skin and
subcutaneous tissue were bluntly dissected to expose muscles. The latissimus dorsi muscle flap
was harvested by transecting it at the level of the 6th rib cranially and below the transverse
process of the spine dorsally. The cranial portion of the external abdominal oblique muscle
was severed from its rib attachment. Both muscles were undermined and elevated till their
attachment to the 11th rib. A combination of the latissimus dorsi and external abdominal
oblique muscles was used to form a large flap that was reversed 180 degrees to cover the
abdominal defect (Fig.
2B). The defect was closed by suturing the muscle flaps with the
residual abdominal wall and hypaxial muscle with 2–0 polydioxanone (PDS II, Ethicon,
Somerville, NJ, U.S.A.), using a simple interrupted pattern (Fig. 2C). Penrose drains were placed, followed by routine closure of
the subcutis and skin. The postoperative pain management was conducted initially with the
constant rate infusion (CRI) of morphine (0.36 mg/kg/hr), lidocaine (1 mg/kg/hr) and ketamine
(0.6 mg/kg/hr) for 3 days, and an additional gabapentin (5 mg/kg PO, TID) for 14 days. The CRI
dosage of each drugs was adjusted according to the patient’s status. After cessation of CRI,
tramadol (4 mg/kg PO, TID) was administered for 11 days. In addition, the animal was also
treated with cephalexin (22 mg/kg PO, TID) and pentoxifylline (10 mg/kg PO, TID) for 14
days.Fourteen days after surgery, a second surgery was performed to repair a small-sized abdominal
hernia that developed at the most caudal dorsal aspect of the muscle flap, and the partial
skin necrosis in the inguinal region (Fig. 3A). The dog was premedicated with dexmedetomidine (65 µg/m2,
IV) and midazolam (0.2 mg/kg, IV) and induced with propofol (1 mg/kg, IV). An endotracheal
tube was placed. Anesthesia was maintained with isoflurane. The dog was placed in left lateral
recumbency. The hernia was approached by incising the skin of the previous surgical incision
line and blunt dissection of the subcutis. Dehiscence at the caudal dorsal end of the
latissimus dorsi muscle flap and herniated intestine could be seen. The rest of the muscle
flap healed well (Fig. 3B). Another incision was
made from the inguinal region to the cranial stifle along the cranial edge of the thigh. The
cranial sartorius muscle was elevated and severed from its distal insertion. It was mobilized
proximally to the level of the vascular pedicle and reversed 180 degrees to cover the
small-sized hernia. After irrigation and restoration of the herniated intestine, the hernia
was closed by suturing the distal portion of the cranial sartorius muscle flap to the defect
with 2–0 polydioxanone in a simple interrupted pattern (Fig. 3C). Penrose drains were placed, followed by routine closure of
the subcutis and skin. The postoperative pain management included CRI of the same drugs for 2
days and then the same dosage of gabapentin and tramadol for 9 days.
Fig. 3.
Repair of a small-sized abdominal hernia resulting from dehiscence in the distal end of
the muscle flap and removal of skin necrosis in the inguinal region. A, The skin
necrosis (black arrows) occurred at the most caudal ventral end of the skin incision. B,
The dehiscence of the muscle flap was located at the most dorsally caudal end of the
flap. A short segment of herniated intestine (black arrow) can be seen. C, The defect
was repaired with an axial pattern of cranial sartorius muscle flap (black arrow).
Repair of a small-sized abdominal hernia resulting from dehiscence in the distal end of
the muscle flap and removal of skin necrosis in the inguinal region. A, The skin
necrosis (black arrows) occurred at the most caudal ventral end of the skin incision. B,
The dehiscence of the muscle flap was located at the most dorsally caudal end of the
flap. A short segment of herniated intestine (black arrow) can be seen. C, The defect
was repaired with an axial pattern of cranial sartorius muscle flap (black arrow).Twenty eight days after the first surgery, a third surgery was carried out to revise a small
vulnerable area from the previously herniated site. After the dog was routinely anesthetized
with the same medication as the previous surgery, positioning was performed in the same way as
the previous surgery. Musculature was exposed after skin incision and blunt dissection of the
subcutaneous tissue of the area. The muscle flap stayed intact with an area that was thinner
than the rest. The thinner musculature was trimmed and sutured. Oral medication after
operation included the same dosage of tramadol, gabapentin and cephalexin for 5 days. The dog
recovered uneventfully afterwards and was in good general health with no sign of tumor
recurrence after 18 months of follow up.Grossly, the tumor invaded and penetrated through the muscle of the abdominal wall (Fig. 4A). Fragmented muscle could be seen within the tumor on cross section. Histopathological
examination of the mass revealed well-differentiated adipocytes infiltrating the skeletal
muscle tissue (Fig.4B). The tumor was excised with
clean margins. A diagnosis of infiltrative lipoma was made.
Fig. 4.
Gross and microscopic appearances of the infiltrative lipoma in the abdominal wall. A,
Gross view from the parietal peritoneum. The tumor had invaded and penetrated through
the muscle of the abdominal wall. B, Histopathological examination revealed that the
well-differentiated adipocytes tumor cells invade the adjacent skeletal muscles and even
replace muscle bundles.
Gross and microscopic appearances of the infiltrative lipoma in the abdominal wall. A,
Gross view from the parietal peritoneum. The tumor had invaded and penetrated through
the muscle of the abdominal wall. B, Histopathological examination revealed that the
well-differentiated adipocytes tumor cells invade the adjacent skeletal muscles and even
replace muscle bundles.In dogs, infiltrative lipomas are uncommon. Infiltrative lipomas are considered benign,
because they do not metastasize. But, as in this case, they are locally invasive and may
infiltrate normal muscle, fascia, nerves, myocardium, joint capsules and bone [2, 3, 5, 6]. Infiltrative
lipomas are composed of well-differentiated adipose cells that are the same as lipomas. Thus,
sometimes, it is impossible to differentiate infiltrative lipomas from lipomas with cytology
and histopathology [2]. For those clinically suspected
infiltrative lipoma cases, CT is a better tool than radiography to assess the infiltrating
nature and extent of this tumor and help make a surgical plan [6]. Except for the cases with prior surgical resection, contrast enhancement will
show peripheral to the tumor possibly due to the prior surgery. Administration of intravenous
contrast medium has no significant benefit for assessment, because there is no contrast
enhancement [6]. However, in a large-sized tumor, such
as in this case, contrast CT scan can provide more accurate assessment of vascular
involvement.Complete surgical excision can be curative and results in long term survival [2], while radiation therapy with measurable disease could
only induce either stable disease or partial response and is better served as an adjuvant
therapy after incomplete surgical resection [7]. In this
case, CT scan was performed to evaluate the extent of tumor and adjacent musculature and plan
surgical margins. The result showed that the infiltrative lipoma was amenable to resection
though it has affected abdominal wall extensively and required further reconstruction after
tumor removal. However, to distinguish an infiltrative lipoma from normal fat tissue is often
very difficult during surgery. This may lead to local recurrence rates of 36–50% [2, 5]. In this case,
the tumor was excised with clean margins. Thus, adjuvant therapy was not recommended.The use of autologous latissimus dorsi, external abdominal oblique and cranial sartorius
muscle flaps with an axial flap pattern respectively to reconstruct the full-thickness of an
abdominal wall defect has been described [1, 9]. However, the abdominal wall defect after tumor removal
in this case was too large to repair with a single muscle flap. Thus, based on the previous
surgical plans, the decision was made to utilize a combination of latissimus dorsi and
external abdominal oblique muscle flaps. The latissimus dorsi muscle is a triangular muscle
covering the most of the dorsal and some of the lateral thoracic wall in the dog [4]. The dominant vascular pedicle of the latissimus dorsi is
the thoracodorsal artery in the proximal portion. Several intercostal arteries supply the
dorsal caudal aspect of the muscle, with the intercostal arteries 6, 7, 10, 11 and 12 being
the most important [10, 12, 13]. The external abdominal oblique
muscle consists of two components, the costal part originates segmentally from the 4th or 5th
rib through the 13th rib, while the lumbar part originates in the thoracolumbar fascia along
the iliocostalis muscle [1, 4]. The major pedicle artery that supplies the external abdominal oblique
muscle is the cranial branch of the cranial abdominal, which supplies the middle zone of the
lateral abdominal wall [1]. The use of an axial or
island flap pattern would not provide enough coverage of the abdominal defect in this case due
to the fact that the mobility of the muscle flaps would be restricted by the pedicle arteries.
Thus, a pedicle flap pattern was used. The two major dominant arteries, the thoracodorsal
artery and the cranial branch of the cranial abdominal artery, which should be preserved for
an axial flap pattern of the latissimus dorsi and external abdominal oblique muscles were
transected during flap harvesting and tumor removal. However, both muscles still received
blood supply from intercostal arteries, although most of the muscle attachments to the ribs
were transected during flap harvesting. The outcome of a combination of the latissimus dorsi
and external abdominal oblique muscle flaps was good with only a small dehiscence that
resulted in a small-sized abdominal hernia. The dehiscence area was located at the most dorsal
caudal end of the flap which received the least blood supply and carried the most tension,
making the area prone to dehiscence. The second surgery was performed to repair the abdominal
hernia with an axial pattern using a cranial sartorius muscle flap, which is supplied by a
single major vascular pedicle. The cranial sartorius muscle flap can be used to cover caudal
abdominal hernia and large inguinal hernia [11].
Consequently, the flap healed well with only a small area of weak muscular tension which did
not lead to hernia or dehiscence.Skin necrosis occurred at the most caudal ventral end of the skin incision after the first
surgery. The skin necrosis may have resulted from transection of the deep circumflex iliac
artery which is the main direct cutaneous vessel that supplies the caudal lateral flank region
[8]. Together with extensive undermining and prolonged
elevation of the skin during surgery, the most distal region may experience poor blood supply
and be prone to necrosis.The vast majority of muscle flaps have been described with axial or island flap pattern with
the pedicle vessels supplying the flap [1, 9, 11]. The mobility
and application of these muscle flaps are limited by pedicle vasculature, and these flaps have
been used to treat ventral or cranial to mid-abdominal wall defects, not caudal abdominal wall
defects [1]. To the best of our knowledge, this is the
first application of a latissimus dorsi muscle flap in combination with an external abdominal
oblique muscle flap using a pedicle flap pattern to cover such a large-sized abdominal wall
defect. Although the major blood supplies were transected during tumor removal and flap
harvesting, the muscle flap healed well with only a minor complication. This technique might
be a novel method for repairing large-sized abdominal wall defects that extend to the caudal
abdomen.
Authors: Marc K Hobert; Christina Brauer; Peter Dziallas; Ingo Gerhauser; Dorothee Algermissen; Andrea Tipold; Veronika M Stein Journal: Can Vet J Date: 2013-01 Impact factor: 1.008