Ultrasonography of soft tissue “oops lesions”
Article information
Abstract
In this article, I would like to define “oops lesions” as soft tissue mass-like lesions that involve surprise or embarrassment for radiologists following the final diagnosis. Examples of “oops lesions” include malignant tumors that appear benign, malignancy-mimicking benign tumors, incorrect identification of epidermal inclusion cysts, and soft tissue pseudotumors. Ultrasonography (US) findings are very helpful in the diagnosis of soft tissue tumors; however, the diagnosis of soft tissue tumors on the basis of US findings alone has some limitations. Therefore, clinical findings, laboratory data, findings from additional imaging modalities, and demographic data of patients should be considered together with US findings.
Introduction
“Oops lesions” could be defined as soft tissue mass-like lesions that involve surprise or embarrassment for radiologists following the final diagnosis. The surprise might represent good or bad news; regardless, it is due to obtaining results that differ from clinical expectations. When a final diagnosis is reached, different responses are possible: “oops” or not; good or bad. If a lesion suspected to be benign is actually confirmed as a malignancy, it is an “oops lesion” and is also sad news. The opposite situation is also an “oops lesion” but is good news. In contrast, when an expected malignancy is confirmed, it is not an “oops lesion” but just sad news. In this article, such surprising or embarrassing cases of soft tissue mass-like lesions will be presented in detail. Examples of “oops lesions” include malignant tumors that appear benign, malignancy-mimicking benign tumors, incorrect identification of epidermal inclusion cysts, and soft tissue pseudotumors. “Oops lesions” could be defined as soft tissue mass-like lesions that involve surprise or embarrassment for radiologists following the final diagnosis. The surprise might represent good or bad news; regardless, it is due to obtaining results that differ from clinical expectations. When a final diagnosis is reached, different responses are possible: “oops” or not; good or bad. If a lesion suspected to be benign is actually confirmed as a malignancy, it is an “oops lesion” and is also sad news. The opposite situation is also an “oops lesion” but is good news. In contrast, when an expected malignancy is confirmed, it is not an “oops lesion” but just sad news. In this article, such surprising or embarrassing cases of soft tissue mass-like lesions will be presented in detail. Examples of “oops lesions” include malignant tumors that appear benign, malignancy-mimicking benign tumors, incorrect identification of epidermal inclusion cysts, and soft tissue pseudotumors.
Benign-Appearing Malignant Tumors
The ultrasonography (US) findings that might suggest benignancy of a soft tissue mass are a small size, superficial location, homogeneous echo pattern, and hypovascularity. However, these findings are not sufficiently reliable to definitively characterize the nature of a lesion [1,2]. US findings can be misleading, since similar findings also occur in synovial sarcoma (Fig. 1), liposarcoma, melanoma, lymphoma, myeloid sarcoma (Fig. 2), and small metastasis (Fig. 3).
Superficial location refers to the subcutaneous tissue and skin above the superficial investing fascia, which separates the subcutaneous tissue layer from the underlying muscle [3]. For soft tissue tumors, large size, deep location, heterogeneous signal intensity and echo, and internal hemorrhage or necrosis suggest the possibility of malignancy rather than a benign tumor [4-7]. To date, the soft tissue sarcoma clinical practice guidelines (National Institute for Health and Care Excellence [NICE] and European Society for Medical Oncology [ESMO]) have used 5 cm as the cut-off size for referral, together with other features such as depth in relation to fascia and increasing size. Other tertiary referral institutions use a 3-5 cm size as a cut-off for risk of malignancy in superficial masses [8].
For superficial masses, there are some factors indicative of malignancy. Unlike deep-seated lesions, size is not an important factor because a significant proportion of superficial malignant tumors measure less than 5 cm in maximal diameter. Fascial edema, skin thickening, skin contact, hemorrhage, and necrosis are highly significant factors indicative of malignancy. Lobulation and peritumoral edema are also significant features [9].
Obtuse angles between the superficial investing fascia and the subcutaneous mass crossing the fascia strongly suggest malignancy [3]. Galant et al. [3] described these fascia-tumor relationships with schematic representation (Fig. 4). Malignant tumors of the subcutaneous compartment have a higher tendency to develop a close relationship with the fascia than benign lesions (Figs. 1B, 5).
Malignancy-Mimicking Benign Mass Lesions
Malignancy should be considered when imaging findings are as follows: complex peri-lesional or intra-lesional changes, internal hemorrhage, hypervascularity, or large-sized mass [1,2,10]. However, these findings can also be present in benign tumors. Ruptured masses or combined infection can cause difficulty in the differential diagnosis of benign and malignant tumors. For cases of ruptured epidermal inclusion cysts, a thick and irregular peripheral rim and septa could be reminiscent of inflammatory lesions such as an abscess or a neoplastic lesion (Fig. 6) [11]. Thus, benign masses can mimic malignancy in cases of post-traumatic hematoma (Fig. 7), myositis ossificans, ruptured benign masses, immature granulomatous lesions, and fibrous lesions (Figs. 8, 9).
Usually, a large-sized, deep-seated mass has a high probability of malignancy; however, this link does not occur in all cases [4-7]. Benign soft tissue tumors such as schwannoma (Fig. 10), nodular fasciitis, lipoma, and hibernoma can be large enough to be misinterpreted as a malignancy.
Incorrect Identification of Epidermal Inclusion Cysts
The US findings of epidermal inclusion cysts are well known. An epidermal inclusion cyst appears as a small, well-defined subcutaneous or cutaneous mass. The sonographic appearance of epidermal inclusion cysts varies with the contents of the cyst, from an anechoic lesion to a hyperechoic, solid-appearing mass [12,13]. The possibility of an epidermal inclusion cyst should be considered when a patient presents with a mass located at the epidermis and subcutaneous tissue that has a demonstrated subtle heterogeneous echo pattern. Most radiologists are familiar with these typical US findings indicating an epidermal inclusion cyst; however, there are sometimes tricky cases that lead to a pathologic diagnosis contrary to expectation that can cause embarrassment.
The imaging findings of an unruptured epidermal inclusion cyst may be similar to other subcutaneous cystic masses, some solid tumors, and vascular lesions. Thus, differential diagnoses include ganglion or bursitis with internal hemorrhage or debris, neurogenic tumors, nodular fasciitis, myxoid tumors, dermatofibrosarcoma protuberans, and hemangioma [11].
The diagnosis of an epidermal inclusion cyst is often confused with perineurioma (an uncommon benign tumor of peripheral nerves composed primarily of perineurial cells [14]), schwannoma (Fig. 11), dermatofibrosarcoma protuberans, and fibrosarcoma arising from dermatofibrosarcoma protuberans (Fig. 12).
Soft Tissue Pseudotumors
Soft tissue pseudotumors include non-neoplastic lesions that are mistaken for neoplastic lesions following imaging studies or clinical examination. Moreover, exophytic bone lesions such as osteochondroma can be misinterpreted as soft tissue tumors. Therefore, many conditions could be involved in a diagnosis of a pseudotumor: inflammatory lesions (cellulitis, abscess, subcutaneous granuloma annulare, parasite infestation); vascular/lymphatic lesions (aneurysm, thrombus, lymphadenitis); posttraumatic lesions such as muscle tear (Fig. 13), muscle herniation, hematoma, fat necrosis, myositis ossificans; a foreign body reaction such as foreign body granuloma (Fig. 14); crystal deposition disease (gouty bursitis); bone tumor (osteochondroma); and normal variation (accessory muscle, sesamoid bone, carpal boss) [15].
Upon imaging, many cases of soft tissue pseudotumors appear cystic in nature and occur at common sites. However, they can show a mixed or solid echo pattern and be detected at unusual sites. In these cases, lesions could show atypical imaging findings and therefore be difficult to diagnose correctly.
Conclusion
US findings are helpful in the diagnosis of soft tissue tumors; however, the diagnosis of soft tissue tumors on the basis of US findings alone has some limitations. Thus, it is not unexpected that “oops lesions” are encountered during clinical practice. Therefore, when a differential diagnosis for a soft tissue mass is made, all available information should be considered, such as demographic data, laboratory findings, and findings from other imaging modalities. In addition, practitioners should be familiar with the variability in US imaging findings.
Notes
No potential conflict of interest relevant to this article was reported.