Soft tissue mass

Last revised by Dr Daniel J Bell on 07 Aug 2022

Soft tissue masses or lesions are a common medical condition seen by primary care physicians, family physicians, surgeons and orthopedists. They include all soft tissue outgrowths benign and malignant 1-3.

Soft tissue masses are very common, with benign lesions being much more frequent than their malignant counterparts, outnumbering them by about 100-150 to one 1-4. Benign soft tissue neoplasms occur with an estimated incidence of approximately 3000/million as opposed to soft tissue sarcomas, which are much less frequent and with an estimated incidence of about 50/million 4. Sarcomas can occur at any age and are generally more common in older people 1,2. However, the ratio of malignant versus benign soft tissue lesions is higher in children because benign lipomas and epidermal cysts are infrequent in that population 1

Many lesions remain unrecognised since not all patients do seek medical attention if they are asymptomatic 2.

Soft tissue masses might be associated with the following 2:

The diagnosis of soft tissue masses is established by a combination of clinical information (comprehensive history and physical examination), imaging findings and histology when indicated 3.

Worrisome features that should raise suspicion for malignancy include 1,3,4:

  • large size >5 cm
  • deep location in relation to the vesting fascia
  • sudden onset and/or rapid growth
  • firm consistency compared to muscle
  • adherence to surrounding structures

Definite diagnosis is usually established histologically 3.

The clinical presentation of soft tissue masses can provide important clues to the etiology of soft tissue masses and important features are the time the mass is present, size, depth, mobility and consistency as well as changes in size and growth rate, the duration, the type of associated symptoms and any prior history of trauma, inflammation/infection or cancer 1-3.

Laboratory studies are usually not of significant benefit because they are non-specific in the evaluation of soft tissue masses 1-3. Inflammatory markers might be abnormal in the setting of an infectious or inflammatory process, uric acid might be elevated in the setting of gout 3.

Certain symptoms and potential corresponding conclusions/clues 1-3:

Complications of soft tissue masses include nerve compression syndromes.

The pathology of soft tissue masses varies with the etiology. Biopsy of suspicious soft tissue masses is technically-demanding and requires careful planning due to the potential complications including needle track seeding. There are two general forms of soft tissue biopsy 2,3:

The needle track should pass through tissue that will be excised during the definite surgery away from major neurovascular structures and in case muscles have to be crossed, those involved by the tumor 1.

The most common etiologies of soft tissue masses are 1-5:

Soft tissue masses can be located anywhere in the body, they can be distinguished based on their depth in superficial and deep soft tissue masses. A superficial location is often but not always indicative of a benign dignity whereas deeply situated masses should raise suspicion for malignancy 2.

Soft tissue masses might be classified into mesenchymal tumors and non-neoplastic soft tissue tumors. Soft tissue neoplasms have been classified by the World Health Organization with regard to the tissue of origin 1,4: see the WHO classification of soft tissue tumors

Certain imaging findings and their corresponding conclusions/clues 3:

Plain radiographs are of limited use for the evaluation of soft tissue masses and usually show only soft tissue shadowing. But they can show calcifications as well as bony involvement in the form of osteolysis, cortical erosion or periosteal reaction.

Ultrasound can help to specify the size, location and mobility of soft tissue masses as well as in the differentiation of cystic versus solid lesions and to determine vascularity and compressibility 3.

Ultrasound may also be used intraoperatively to guide biopsy or excision 2.

CT can identify calcifications and osseous involvement. It can help in the differentiation of calcifications from ossifications thus chondroid matrix from an osteoid matrix or characterize masses in patients who cannot undergo MRI 2. It is also very useful for the evaluation of soft tissue masses of the trunk and in the staging of malignant disease 4.

MRI is considered the imaging modality of choice for the evaluation and tissue characterization of soft tissue masses 1-4. It can aid in the differentiation of watery, fatty and solid tumor components and with the administration of contrast in the differentiation of cystic lesions and myxoid neoplasms 3. It helps in the localization of tumors within the different anatomic compartments and the determination of their relationship to neurovascular structures and the muscular fascia 2 and can be used to guide biopsy 3.

Certain MR imaging characteristics of soft tissue masses and corresponding conclusions/clues 3:

  • low T1, high T2 with rim enhancement: cystic lesion e.g. ganglion cyst, epidermal inclusion cyst
  • low T1, high T2 with a homogeneous enhancement: myxoid lesion e.g. intramuscular myxoma
  • low T1, high T2 with a heterogeneous enhancement: myxoid lesion e.g. myxoid liposarcoma
  • early, vivid enhancement: viable solid tumor
  • delayed enhancement: granulation tissue
  • blooming artifact: the presence of hemosiderin e.g. in hematoma, tenosynovial giant cell tumor, hemangioma

PET-CT can provide information about the metabolic activity of soft tissue tumors and can be used in the evaluation of treatment and the detection of tumor recurrence 2,3.

The radiological report should include a description of the following points:

  • form, location and size, consistency (cystic versus solid)
  • tumor margins
  • relation to the muscular fascia
  • relationship to bones, tendons and joints
  • relationship to local nerves and vessels

Management of soft tissue masses requires careful planning and often consists of resection of the mass with or without adjuvant therapy. Nevertheless, a high percentage of malignant soft tissue masses end up undergoing unplanned resection potentially leading to higher local recurrence rates and other complications 1.

Four general types of oncologic resection procedures are performed 2,3:

  • intralesional excision: e.g. for hematoma 
  • marginal excision: e.g. for lipomas, tenosynovial giant cell tumors, neurofibromas
  • wide resection: for locally aggressive tumors such as sarcomas
  • radical resection: rarely required

Depending on the etiology of the soft tissue mass and the type of resection treatment might be combined with different adjuvant or neoadjuvant therapies including local treatment such as cryotherapy or radiofrequency ablation, radiation therapy and chemotherapy 2,4.

  • should be done by an oncologic surgeon and ideally by the same surgeon who will definitely treat the patient or perform the excision due to potential complications including tumor cell spreading 2,3
  • should be performed through a single track that can be completely excised during definitive tumor resection away from nerves and vascular structures 2-4
  • should involve a minimal amount of the overlying skin 1

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Cases and figures

  • Case 1: soft tissue hematoma
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  • Case 2: soft tissue lipoma
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  • Case 3: ganglion cyst
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  • Case 4: soft tissue hemangioma
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  • Case 5: intramuscular myxoma
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  • Case 6: tenosynovial giant cell tumor
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  • Case 8: hemorrhagic superficial infrapatellar bursitis
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  • Case 7: soft-tissue abscess
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  • Case 9: epidermal inclusion cyst
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  • Case 10: atypical lipomatous tumor
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  • Case 11: foreign body granuloma
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  • Case 12: retroperitoneal desmoid tumor
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  • Case 13: extraskeletal Ewing sarcoma
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