INTRODUCTION
Lipomas are benign neoplasms histologically characterized by the presence of mature
adipocytes with small nuclei pushed to the cellular periphery by lipid droplets1,2. The tumor presents variable amounts of fibrous stroma, sometimes condensed in the
lesion’s periphery, forming an incomplete capsule (pseudocapsule)3. Lipomas are the most frequent benign soft tissue mesenchymal tumors4,5,6, with an estimated incidence in the adult population of 0.21% to 0.5% and a prevalence
of 10%7,8,9,10,11.
Lipomas are usually subcutaneous, but they can be located anywhere in the body that
contains adipose tissue, including viscera, cavities, central nervous system, gastrointestinal
tract, muscles and joints1,4,5,8.0 About 80% are smaller than 5 cm in diameter; however, some can reach more than
20 cm and weigh several kilograms, configuring the so-called giant lipomas5. Diagnosis of lipomas is clinical-histopathological1, and treatment is usually surgical7.
According to Sanchez et al.12, for a lipoma to be considered giant (GL), it must have a minimum of 10 cm in one
of its dimensions or weigh at least 1000 grams. The largest reported GL in the world
was 22.7kg5,12 and, in Brazil, 22.0kg8.
GL are uncommon in clinical practice (< 5% of all lipomas)4. Although rare, they have medical relevance, as they can affect any body region and
are diagnosed in advanced stages in which there is aesthetic and/ or functional impairment4,5,6,9. They can be confused with malignant soft tissue neoplasms11,13. Finally, GL’s natural history is still not exactly known4.
OBJECTIVE
This work aims to report a case of GL treated with elliptical excision by the plastic
surgery team at Hospital Roberto Santos (Salvador/BA) in 2016.
CASE REPORT
The report followed the recommendations of SCARE (Statement Consensus Based Surgical
Case Report Guidelines 2018). The retrospective study was approved by the Medical
Ethics Committee (CAAE 46603221.7.0000.5028, opinion 4.793.410).
Male, 62 years old, faioderm, farmer, 74kg, 1.80m, with a voluminous dorsal tumor
that started 20 years earlier as a small bulge of slow and progressive growth, reaching
its current dimensions five years ago. Since then, the patient has experienced local
pain, grotesque deformity and social isolation.
On examination, a hemispherical mobile mass measuring 35 cm in diameter was observed
in the proximal third of the back, not adhering to deep planes, painless, softened,
with normal overlying skin (Figure 1A). No abnormalities were found in family history, general physical examination or
laboratory evaluation (blood count, coagulogram, blood glucose, urinalysis, urea,
creatinine, electrolytes and ECG).
Multislice CT of the chest (Toshiba Aquilion 8-slice) revealed a multiseptated subcutaneous
mass with fat density, measuring 21.0 x 23.1 cm, located in the upper third of the
dorsum compatible with GL. The examination did not detect compression of thoracic
or cervical structures.
The treatment instituted was surgical excision. Thirty minutes before the procedure,
intravenous antibiotic prophylaxis (cefazolin, 2,000mg) was performed. However, drug
thromboprophylaxis was not performed due to the low risk of developing intraoperative
thrombosis (according to the criteria and recommendations proposed by Moulim et al.)14.
Under general anesthesia, a 30cm x 5cm transverse elliptical incision was made over
the tumor dome, which was dissected from the surrounding subcutaneous and muscular
tissues. The mass had a greasy appearance and consistency and had internal septa and
a fibrous external capsule forming a cleavage plane (except on the deep side of the
tumor) that facilitated dissection and resulted in limited bleeding. A massive multilobed
lipomatous tumor was removed (Figure 1B), showing its paravertebral emergence from the middle part of the left trapezius
(Figure 1B - arrow). After hemostasis, excess skin was removed and closed with an inverted W
suture (Figure 1C). Stitches were made with 2-0 black mononylon thread in subdermal (simple inverted)
and intradermal (continuous cuticular suture) planes.
Figure 1 - Giant lipoma. A: Preoperative aspect; B: Elliptical excision, arrow: tumor origin; C: Immediate postoperative period; D: 6-month postoperative period; E: Postoperative period of 5 years.
Figure 1 - Giant lipoma. A: Preoperative aspect; B: Elliptical excision, arrow: tumor origin; C: Immediate postoperative period; D: 6-month postoperative period; E: Postoperative period of 5 years.
The entire procedure, including skin suturing, lasted four hours and thirty minutes
and was performed by a team coordinated by a plastic surgeon with 20 years of training
in the specialty. The patient was discharged from the hospital after seven days of
uncomplicated hospitalization. Postoperatively, he was instructed to apply wet gauze
dressings and antibiotic ointment (bacitracin and neomycin) until complete healing,
followed up on an outpatient basis by the surgical team weekly for the first month
and then every two months.
Histopathological analysis revealed a giant lipoma measuring 2881 grams, measuring
29.0 x 26.0 x 6.0 cm. In the sixth month evaluation, the operated region remained
flat, with a slightly hypertrophic surgical scar (5mm, Figure 1D) and slightly depressed in the 5-year evaluation (Figure 1E). The patient and the surgical team considered the final result (aesthetic and functional)
excellent.
DISCUSSION
The current report presents a typical patient with GL: a male in the sixth decade
of life with a slow-growing tumor and unrecognizable etiology1,4,5,6,9,11,13. The lipoma’s dimensions and mass (2881g), although reduced concerning the bulkier
GLs described, fit into the most common range described for GL (493.75g to 3.8 kg-cm)11. The preoperative diagnosis of the present GL was clinical, as the lesion had the
usual characteristics (soft consistency, slow growth, mobility and intact overlying
skin, absence of pain and systemic manifestations15).
The GL presented was an example of an inter-muscular lipoma related to the trapezius.
Interestingly, the first subfascial lipoma described in the literature (in 1856, by
Padget) also originated from the muscle3. When growing, the GL of the current report
caused great expansion of the overlying skin, so there was a need to remove a large
ellipse of redundant integument after removing the mass. The final suture was placed
in a zigzag pattern to prevent retractable straight scar formation. The long surgical
time was attributed to the large size of the tumor and the difficulty in releasing
the GL attached bilaterally to the underlying trapezius due to the absence of an identifiable
fibrous capsule in the area of contact with the muscle.
The GL described did not present compressive symptoms, so the excision was performed
to allow a differential diagnosis with liposarcomas and, above all, for cosmetic reasons.
Rydholm & Berg reported that lesions >10 cm have a 25-fold greater risk of malignancy
than lesions <5 cm. This study alerts to the need for surgical removal of the GL even
in the absence of manifestations suggestive of malignancy7. Despite the compressive problems they may cause, paradoxically, most lipomas are
removed for aesthetic reasons4. As in a current report, the indication can be important
for correcting gross deformities, contributing to the reintegration of patients socially
marginalized because of the deformity.
The present report’s lack of postoperative adverse effects seems to be an exceptional
finding, since immediate complications after GL resection are frequent, including
paresthesias, skin necrosis, surgical wound infections, lower limb varicose veins
and pulmonary complications8. Late postoperative complications have not been reported5. Post-surgical relapses are considered low for the intermuscular variant and slightly
higher for the intramuscular type, especially when the affected muscles are preserved4,11,13.
CONCLUSION
The presented GL was removed without complications and with excellent aesthetic and
functional results.
REFERENCES
1. Nigri G, Dente M, Valabrega S, Beccaria G, Aurello P, D’Angelo F, et al. Giant inframuscular
lipoma disclosed 14 years after a blunt trauma: a case report. J Med Case Rep. 2008;2:318.
2. Righi A, Pantalone O, Tagliaferri G. Giant lipoma of the thigh: a case report. J Ultrasound.
2012;15(2):124-6.
3. Kindblom LG, Angervall L, Stener B, Wickbom I. Intermuscular and intramuscular lipomas
and hibernomas. A clinical, roentgenologic, histologic, and prognostic study of 46
cases. Cancer. 1974;33(3):754-62.
4. Daher JC, Amaral JDLG, Cammarota MC, Benedik Neto A, de Faria CADC. Lipoma gigante
de Membro inferior com repercussão no sistema vascular. Rev Bras Cir Plást. 2013;28(3):522-5.
5. Accetta P, Accetta I, Vassallo EC, Milman M, Souza AM, Accetta AC. Lipomas gigantes.
Rev Col Bras Cir. 1998;25(5):364-5.
6. Hakim E, Kolander Y, Meller Y, Moses M, Sagi A. Gigantic lipomas. Plast Reconstr Surg.
1994;94(2):369-71.
7. Rydholm A, Berg NO. Size, site and clinical incidence of lipoma. Factors in the differential
diagnosis of lipoma and sarcoma. Acta Orthop Scand. 1983;54(6):929-34.
8. Mello D F, Manica MZ, Helene Júnior A. Lipomas gigantes: série de 14 casos. Rev Bras
Cir Plást. 2015;30(1):33-7.
9. Mello D, Helene A Jr. Lipoma subgaleal gigante: relato de caso. Rev Bras Cir Craniomaxilofac.
2010;13(3):180-2.
10. Mescon H. Lipoma in clinical dermatology. Clin Dermatol. 1991;4:1-2.
11. Terzioglu A, Tuncali D, Yuksel A, Bingul F, Aslan G. Giant Lipomas: A series of 12
consecutive cases and a giant liposarcoma of the thigh. Dermatol Surg. 2004;30(3):463-7.
12. Sanchez MR, Golomb FM, Moy JA, Potozkin JR. Giant lipoma: case report and review of
the literature. J Am Acad Dermatol. 1993;28(2 Pt 1):266-8.
13. d’Alessandro G, Nunes T, Lajner A, Beirigo M, Porto O, Pinto W. Lipoma intermuscular
gigante: relato de caso. Rev Bras Cir Plást. 2008;23(3):226-8.
14. Moulim JL, Sobreira ML, Malgor RD, de Abreu CR, de Araújo ESF, Palhares Neto AA. Estudo
comparativo entre protocolos para profilaxia da trombose venosa profunda: uma nova
proposta. Rev Bras Cir Plást. 2010;25(3):415-22.
15. Singh M, Saxena A, Kumar L, Karande SK, Kolhe Y. Giant Lipoma of Posterior Cervical
Region. Case Rep Surg. 2014;2014:289383.
1. Instituto de Ciências da Saúde, Universidade Federal da Bahia, Programa de Pós-Graduação
em Processos Interativos de Órgãos e Sistemas, Salvador, BA, Brazil.
2. Hospital Geral Roberto Santos, Cirurgia Geral, Salvador, BA, Brazil.
Corresponding author: Sandro Cilindro de Souza ICS-UFBA, Av. Reitor Miguel Calmon, sala 110, 1º Andar, Vale do Canela, Salvador,
BA, Brazil Zip Code: 40110-902 E-mail: sandrocilin@gmail.com.br
Article received: April 26, 2021.
Article accepted: October 15, 2021.
Conflicts of interest: none.
Institution: Hospital Geral Roberto Santos, Salvador, BA, Brazil.