Literature DB >> 34912680

Periauricular Angiolipoma: A Case Report.

Gholamreza Motazedian1, Ali Khojasteh1, Fatemeh Salari2, Mohammad Hossein Anbardar3.   

Abstract

Angiolipoma is an uncommon benign fatty tumor which is a variant of lipoma. Microscopic studies on angiolipoma show that it includes the mature lipocytes and blood vessels. Infiltrating angiolipoma is an un-capsulated angiolipoma and, due to penetration into the surrounding structures, complete excision of the tumor is difficult. According to previous studies, the relapse rate of the infiltrating angiolipoma after surgical intervention is 35-50%. Infiltrating angiolipoma is rarely seen in the head and neck region and often occurs in the trunk and limbs. In this study, we report a 10-year-old boy with periauricular infiltrating angiolipoma who underwent surgery. After surgery, the patient developed transient left frontal branch palsy, but recovery was excellent and after one year there is no relapse.

Entities:  

Keywords:  Angiolipoma; Periauricular region

Year:  2021        PMID: 34912680      PMCID: PMC8662692          DOI: 10.29252/wjps.10.3.134

Source DB:  PubMed          Journal:  World J Plast Surg        ISSN: 2228-7914


INTRODUCTION

Lipomas are fatty tumors and 5-17% of these tumors are angiolipomas(1). Angiolipoma is a variant of lipoma that includes mature lipocyts and blood vessels(2-6). Infiltrating angiolipoma are often placed deeper than the non-infiltrating form(1, 7). Infiltrating angiolipoma usually occurs in the trunk and limbs and is rarely seen in the head and neck region. Location of the tumor is a major factor in determining its prognosis(1). We present a patient with infiltrating angiolipoma in the periauricular region that underwent surgery.

CASE REPORT

This study was conducted in August 2020 at Amiralmomenin hospital in Shiraz. A 10-year old boy presented with a mass on the left periauricular region with bluish discoloration during exercises (Figure 1). The patient had no history of trauma and infectious diseases. Physical exam showed a left periauricular painless subcutaneous mass. The facial magnetic resonance imaging (MRI) revealed ill-defined soft tissue mass in the left periauricular region. The tumor had hyper-intense signal on T2 weighted sequences and isointense signal on T1 weighted sequences (Figure 2). Fine needle aspiration was not diagnostic. Surgical excision of the un-capsulated mass was performed through periauricular incision under general anesthesia and loupe magnification. The specimen was sent for pathologic evaluation and infiltrating angiolipoma was reported (Figure 3). After surgery, the patient developed transient left frontal branch palsy, but recovery was excellent and after one year there is now no relapse.
Fig. 1

A 10-year-old boy with a mass on the left periauricular region

Fig. 2

MRI revealed an ill-defined soft tissue mass

Fig. 3

Section shows mature lipocyts and blood vessels indicating infiltrating angiolipoma

INFORMED CONSENT

Informed consent was obtained from the patient.(Ethical Code: IR.SUMS.REC.1400.405).

DISCUSSION

Angiolipoma is a variant of lipoma that includes mature lipocyts and blood vessels(2-6). In different cases, the ratio of the lipocyt to the blood vessels varies, but in most of them the percentage of lipocyts is higher than blood vessels (4, 8). In terms of having or not having a capsule, they are divided into two categories: encapsulated (circumscribed) and un-capsulated (infiltrating) angiolipoma which penetrates the surrounding structures (9). Infiltrating angiolipoma usually occurs in the trunk and limbs and is rarely seen in the head and neck region. Location of the tumor is a major factor in determining its prognosis (7). Angiolipomas usually happen sporadically, but a few cases have a family history of angiolipoma, and the inheritance pattern in these cases is autosomal recessive or in very rare cases autosomal-dominant pattern (5, 10). Also, in a study that examined the karyotype of three cases of angiolipoma, the researchers concluded that all three cases had abnormal karyotypes with loss or structural rearrangement of chromosome 13(8). Histopathologic studies are required for definitive diagnosis of angiolipoma from other soft tissue tumors such as hemangioma, myxolipoma, and Kaposi’s sarcoma; magnetic resonance imaging (MRI) can be useful in evaluation of the tumor expansion and preoperative diagnosis (5, 11). Surgical excision is the best treatment for both encapsulated and un-capsulated angiolipomas (2, 3, 7). Because infiltrating angiolipoma often penetrates the surrounding tissues, complete resection of the tumor may damage the surrounding structures (5, 7). In the maxillofacial region, due to the existence of many vital structures, magnified operation is necessary to prevent damage to these structures, but in some situations sacrificing a branch of nerves is inevitable (12). According to previous studies, the relapse rate of infiltrating angiolipoma is 35-50%(6). Two possible causes of the recurrence of infiltrating angiolipoma after surgery are incorrect evaluation of the extent of the tumor and inadequate tumor resection during surgery (5). A 10-year-old boy with a mass on the left periauricular region MRI revealed an ill-defined soft tissue mass Section shows mature lipocyts and blood vessels indicating infiltrating angiolipoma

CONCLUSION

Angiolipoma is a variant of lipoma considered as one of differential diagnoses of the head and neck mass for proper treatment.

CONFLICT OF INTEREST

The authors declare no conflict of interest.
  12 in total

1.  Successful treatment with interferon alfa in infiltrating angiolipoma: a case presenting with Kasabach-Merritt syndrome.

Authors:  C Akyüz; S Emir; M Büyükpamukçu; N Büyükpamukçu; M Cağlar; G Kale; U Calişkan
Journal:  Arch Dis Child       Date:  2003-01       Impact factor: 3.791

2.  Giant angiolipoma of the arm in an elderly patient.

Authors:  P E Papakonstantinou; P Korkolopoulou; D Lassithiotakis; E D Lolis
Journal:  Ann R Coll Surg Engl       Date:  2016-05-31       Impact factor: 1.891

3.  Infiltrating angiolipoma of the cheek.

Authors:  Vandana S Shah; M Harish; Jayanti R Patel; Nidhi Shah
Journal:  BMJ Case Rep       Date:  2013-09-06

4.  Consistent Involvement of Chromosome 13 in Angiolipoma.

Authors:  Ioannis Panagopoulos; Ludmila Gorunova; Kristin Andersen; Ingvild Lobmaier; Bodil Bjerkehagen; Sverre Heim
Journal:  Cancer Genomics Proteomics       Date:  2018 Jan-Feb       Impact factor: 4.069

Review 5.  Angiolipoma of the cheek: report of a case.

Authors:  M H Ali; F el-Zuebi
Journal:  J Oral Maxillofac Surg       Date:  1996-02       Impact factor: 1.895

6.  Non Infiltrating Angiolipoma of the Palate in Geriatric Patient: A Case Report with Review of Literature.

Authors:  Deepak Chandrasekaran; Ravindran Chinnaswami; Malathi Narasimhan; Annie Evangelin Nithia Kumar; Parthasarathy Natarajan
Journal:  J Clin Diagn Res       Date:  2016-01-01

7.  Autosomal-dominant familial angiolipomatosis.

Authors:  George Garib; Gene P Siegal; Aleodor A Andea
Journal:  Cutis       Date:  2015-01

8.  Cavernous Hemangioma of Temporalis Muscle: A Case Report.

Authors:  Gholamreza Motazedian; Ali Khojasteh; Nasrin Motazedian; Mohammad Hossein Anbardar
Journal:  World J Plast Surg       Date:  2020-01

9.  Infiltrating angiolipoma of the lower lip: A case report and literature review.

Authors:  Yuichi Ohnishi; Masahiro Watanabe; Tomoko Fujii; Hiroki Yasui; Hirohito Kubo; Kenji Kakudo
Journal:  Oncol Lett       Date:  2014-11-25       Impact factor: 2.967

10.  Angiolipoma in the Head and Neck: Imaging, Diagnosis and Management.

Authors:  Vadim Reiser; Bahaa Haj Yahya; Gavriel Chaushu; Ilana Kaplan; Yafit Hamzani
Journal:  Medicina (Kaunas)       Date:  2020-06-10       Impact factor: 2.430

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.