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Nodular Fasciitis
Nodular Fasciitis
Nodular Fasciitis
Áine O’Brien
Introduction
Nodular fasciitis is a rare soft tissue tumor that occurs
in the fascia of muscles. It is composed of
myofibroblasts. The fascia is the connective tissue that
connects muscles. This tumour is non-cancerous and
does not spread.
The most common sites for this tumor to occur is on the
head, neck, arms, legs or torso.
2
Characteristics of nodular fasciitis
NF occurs predominantly in young to middle-aged adults.
It
typically presents as a fast-growing nodule that reaches 2 to 3
cm in size within a few weeks.
Themost common site is the upper extremities, followed by the
trunk, head and neck region.
However, the lesion can occur in unusual locations such as in a
salivary gland, the breast, the mesentery, and the vulva.
3
Characteristics of nodular fasciitis
Cranial fasciitis, which is a
distinctive form of nodular
In children, the head and neck Nodular fasciitis can occur in
fasciitis, can occur in infants.
are common locations for suprafascial, intrafascial, and
This involves the soft tissue of
nodular fasciitis. subfascial locations.
the scalp and may invade the
underlying bone.
4
Relatively well-circumscribed fascia-based nodule
of the anterior aspect of the right thigh measuring A large well encapsulated mass lesion
28 x 26 x 20 mm. It elicits an isosignal to muscle is seen subcutaneously in upper arm.
on T1, heterogeneous high signal on T2 with vivid
homogeneous enhancement on postcontrast
sequences. Moderate infiltration of the
surrounding fatty tissue with no extension to the
adjacent muscles.
5
Symptoms
A fast-growing lump
Firm to touch
Usually painless but can be tender
Solid mass
Mobility can be affected depending on location
Can cause pain if lump presses against a nerve
6
Aetiology has been associated with previous
trauma in 5–10% of the cases. It has also been
associated with a hyper-response mechanism
which triggers an increase in mitotic activity in
certain predisposed individuals.
It is not usually known why nodular Fasciitis
occurs but is can be mistaken for:
Aetiology Fibromatosis
Schwannoma
Harmless nerve sheath tumor
Synovial sarcoma
Dermatofibrosarcoma protuberans
Myxofibrosarcoma
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Imaging - MRI
Sarcoma
Nodular Fasciitis
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Histology
NF presents as a proliferation of spindle cells which are arranged in short S-shaped assortments within a
myxoid stroma that have small capillaries and extravasated erythrocytes.
Histologically, nodular fasciitis is classified into three subtypes: myxoid or reactive (type I), cellular (type
II), and fibrous (type III); however, the lesions may present characteristics of different subtypes,
corresponding to progressive phases of the same disease.
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Treatment
Surgical Removal
Corticosteroid injection
When spontaneous regression occurs, regular check-ups
should be carried out.
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Breast Nodular fasciitis
The WHO categorised nodular fasciitis of the breast as a It can also be regular, oval or round with well-
benign mesenchymal breast tumour. defined margins.
This tumour is often painless, palpable and can mimic a On an ultrasound scan, the margins are most often
malignant neoplasm.
irregular, and the vascularity is generally minimal or
Clinical manifestations, poor specificity of imaging and completely absent.
cyto-histological features can hinder the differential
diagnosis. This negatively impacts the therapeutic strategy. Breast nodular fasciitis may resemble several other
breast lesions. These can present similar radiological
Nodular fasciitis in this location is very rare.
or even pathological features. Examples include:
The appearance of breast fasciitis on a mammogram is a
fibromatosis, myofibroblastoma, inflammatory
dense, irregular or spiculated nodule, that has poorly
myofibroblastic tumour, metaplastic carcinoma and
defined margins.
sarcoma.
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References
• https://my.clevelandclinic.org/health/diseases/23510-nodular-fasciitis
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Lu L, Lao IW, Liu X, Yu L, Wang J. Nodular fasciitis: a retrospective study of 272 cases from China with
clinicopathologic and radiologic correlation. Ann Diagn Pathol. 2015 Jun;19(3):180-5. doi:
10.1016/j.anndiagpath.2015.03.013. Epub 2015 Apr 6. PMID: 25890487.
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