Reshadi Habib, Rouhani Alireza, Mohajerzadeh Saeid, Moosa Marvan, Elmi Asghar
Habib Reshadi MD, Alireza Rouhani MD, Saeid Mohajerzadeh MD, Orthopedic Department, Shohada Hospital, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Arch Bone Jt Surg. 2014 Jun;2(2):106-10. Epub 2014 Jun 15.
Although the majority of soft tissue masses are benign, it is important to consider malignancy in differential diagnoses. Because most soft tissue sarcomas present as a painless mass, clinicians must watch for signs suggestive of malignancy, including large size, rapid growth, and site deep into the deep fascia. The purpose of this study was to determine the relative prevalence according to sex and age, site of tumor, skeletal distribution, and treatment (surgery, chemotherapy and radiotherapy) before and after surgery, and ascertain the relative frequency of these tumors in specific anatomic sites and age groups based on pathological studies.
A total of 308 patients, with a musculoskeletal tumor were evaluated retrospectively. All of the patients enrolled into this study were referred to the Beirouni Hospital of Damascus University with a proven diagnosis of malignant soft tissue tumors from the beginning of January 2008 until the end of 2010. The prevalence of the malignant soft tissue tumors in these patients was analyzed. For purposes of analysis, all lesions were placed in 1 of 9 categories: hand and wrist, forearm, humorous (arm), proximal limb girdle (axilla and shoulder), foot and ankle, thigh, hip and buttocks region, trunk, and other lesions. Age and sex also were recorded.
MALIGNANT TUMORS CONSISTED OF SEVEN DIAGNOSTIC CATEGORIES: malignant fibrous histiocytoma (23%), liposarcoma (22%), rhabdomyosarcoma (9%), leiomyosarcoma (8%), malignant schwannoma (5%), dermatofibrosarcoma protuberans (5%), synovial sarcoma (10%), fibrosarcoma (13%), extraskeletal chondrosarcoma (1%), and extraskeletal Ewing sarcoma (4%).
Despite the multitude of pathologic possibilities, most malignant soft-tissue tumors are classified into a small number of diagnoses. These may be further defined when the site of the lesion and the age of the patient are considered. Knowledge of tumor prevalence will assist radiologists in establishing a suitably ordered differential diagnosis when a soft-tissue tumor has a nonspecific radiologic appearance.
尽管大多数软组织肿块是良性的,但在鉴别诊断中考虑恶性肿瘤很重要。由于大多数软组织肉瘤表现为无痛性肿块,临床医生必须留意提示恶性肿瘤的迹象,包括体积大、生长迅速以及位于深筋膜深层。本研究的目的是确定根据性别和年龄、肿瘤部位、骨骼分布以及手术前后的治疗(手术、化疗和放疗)的相对患病率,并根据病理研究确定这些肿瘤在特定解剖部位和年龄组中的相对频率。
回顾性评估了308例患有肌肉骨骼肿瘤的患者。从2008年1月初至2010年底,所有纳入本研究的患者均被转诊至大马士革大学贝鲁尼医院,确诊为恶性软组织肿瘤。分析了这些患者中恶性软组织肿瘤的患病率。为了进行分析,将所有病变分为9类中的1类:手和腕部、前臂、肱骨(手臂)、近端肢体带(腋窝和肩部)、足和踝部、大腿、髋部和臀部区域、躯干以及其他病变。还记录了年龄和性别。
恶性肿瘤包括七个诊断类别:恶性纤维组织细胞瘤(23%)、脂肪肉瘤(22%)、横纹肌肉瘤(9%)、平滑肌肉瘤(8%)、恶性神经鞘瘤(5%)、隆突性皮肤纤维肉瘤(5%)、滑膜肉瘤(10%)、纤维肉瘤(13%)、骨外软骨肉瘤(1%)和骨外尤文肉瘤(4%)。
尽管存在多种病理可能性,但大多数恶性软组织肿瘤可归为少数几种诊断。当考虑病变部位和患者年龄时,这些诊断可能会进一步明确。了解肿瘤患病率将有助于放射科医生在软组织肿瘤具有非特异性放射学表现时建立适当的鉴别诊断顺序。