Liposarcomas are generally rare and their incidence does not exceed 2.5 cases/million inhabitants/year [1] . This rarity is relative because liposarcomas still represent 14% to 18% of all malignant tumors of the soft tissues [2] . They are the most common soft tissue sarcomas [3] . They predominate at the level of the limbs (50%) but can also develop at the level of the trunk (33%) [2] . Because of the unusual age, we report a case of large liposarcoma of the dorsal surface of the trunk in a 35-year old patient.

A 35-year-old man without a notable patient history was admitted for a mass of the back discovered three years before without any notion of trauma. The patient affirms the recent appearance of an induration motivating the consultation. There were no associated signs such rectorrhagia, hematemesis, emaciation, pain.

The physical examination finds a patient in good general condition. Locally, there is a swelling of the right lateral part of the 1/3 middle part of the back. It is an oval swelling of 25 cm long axis (Figure 1, Figure 2). The surrounding skin looks normal. At palpation the swelling is firm, poorly limited and mobile compared to superficial and deep planes and not painful. The axillary and cervical ganglion areas are free of any adenopathies. The rest of the somatic examination was normal. The chest CT scan (Figure 3) shows images in favor of a fat mass of the right chest wall of benign shape. The patient underwent tumor excision under general anesthesia. The incision was linear compared to the mass. After opening the fascia and dissecting the fibers of the large dorsal muscle, the tumor was exposed presenting as a fatty mass. Excision of the entire tumor and its capsule is performed (Figure 4). The continuations were simple with no tumor recurrence to date (18 months).

The pathological examination of the operative specimen shows a globally lobulated tumor proliferation. The lobules are surrounded by fibrous septa of variable thickness. Within the intra-lobular mature adipocyte plaques, there is the presence of numerous lipoblasts and atypical adipose cells with multi-vacuolar cytoplasm with a nucleolarhyperchromatic nucleus and notch-like appearance. No tumor necrosis was noted and this proliferation is surrounded by a thin fibrous capsule. The diagnosis of well differentiated liposarcoma of sclerosing type was made. The patient was introduced to the multidisciplinary oncology staff.

First described by Virchow in 1860, liposarcoma is a rare mesenchymal tumor [1] . However, it is the most common soft tissue sarcoma [3] [4] . It most often affects the adult subject. Some authors find it between 50 and 70 years [2] [5] , others delimits a period of 40 to 60 years [3] , therefore affects the adult after the fourth decade with a male predominance. In our case it’s a young adult of 35 years, what makes the peculiarity. According to some authors, liposarcoma develops at the expense of primitive mesenchymal cells rather than at the expense of adipocytes. It would never develop on a lipoma or pre-existing lipomatosis [3] [5] . Indeed genetic or traumatic factors could promote this differentiation of adipocytes [6] . Clinically, liposarcoma is in the form of a bulky mass generally greater than 5 cm in size. For this purpose several authors report a parallelism between the size of the fat tumors and their malignancy with up to 74% sensitivity of malignancy if the size is greater than 5 cm [7] [8] . This tumoral mass is of variable aspect, most often nodular well limited [1] [3] . The deterioration of the general state and the pains are rare and are found only at the end of evolution [2] . Any fat tumor having a size more than 5 cm must therefore receive special attention even before the fourth decade. Pathologically, there are five types of liposarcoma; well differentiated, myxoid, round cell, pleomorphic, dedifferentiated. Liposarcomas of themyxoid type and of well-differentiated type are the most frequent. [3] [6] [9] [10] . The well-differentiated liposarcomas are tumors of low grade malignancy looking like lipomas hence the name “lipoma like” [2] with the presence of some lipoblasts [3] as shown by the pathological examination of our operative specimen. Whatever histological type, surgical excision is the key to treatment. It may, in some cases be supplemented by radiotherapy and sometimes chemotherapy especially in multiple metastases or inoperable cases. The prognosis of liposarcoma generally depends on the histological type, the size of the tumor and its extent at the time of diagnosis [2] . In all cases, recurrences are frequent and usually occur within 24 months after surgical treatment. Metastases are possible; the most common are pulmonary and hepatic and are haematogenous. However, liposarcoma of well-differentiated type is of better prognosis with a survival rate of more than 50% at 10 years [2] [3] . In addition, adequate initial surgical management combined when indicated with a well-managed adjuvant treatment can reduce recurrences.

Any fat tumor having a size more than 5 cm must therefore receive special attention even before the fourth decade.

We received the patient’s consent.

The authors declare no conflicts of interest regarding the publication of this paper.

Maïga, A., Diakité, I., Bah, A., Bathio, T., Diassana, B., Diallo, A.B., Traoré, A.A., Diallo, M., Dembélé, B.T., Sidibé, Y., Saadé, O.H., Kanté, M., Konaté, M., Dembélé, S., Samaké, M., Togo, A., Traoré, A. and Diallo, G. (2019) Liposarcoma of the Back: Case Report. Surgical Science, 10, 141-145. https://doi.org/10.4236/ss.2019.104017