Breast hamartoma, also
known as fibroadenolipoma, is a benign type of breast tumour. It was first
described by Arrigoni et al. in 1971 as a well-circumscribed lesion composed of
benign epithelial cells, adipose, and fibrous tissues. Women older than 40 years
of age are most likely to be affected [1]. Hamartoma can occur in younger and
older patients; however, this tumour will always develop before menopause [2].
Additionally, Venkatesh and Harish reported a case of it occurring in a
14-year-old girl. This shows that it can happen at any age [3]. Although
hamartoma typically grows slowly, a faster growth rate was reported during
pregnancy and lactation. Immunohistochemical similarities to normal gland
tissue play a major role (positive for hormone receptors and KI67). A few rare
cases have also been reported in males and in ectopic mammary tissue observed
in inguinal or axillary areas [4].

Figure
2:
Breast MRI: (A) T1 and (B) T2WI showed a well-circumscribed oval mass of the
left breast, surrounded by a thin capsule, with a fat and glandular component;
(C) On dynamic post-contrast T1WI FS subtracted images, the mass did not
enhance except for some foci showing slow progressive enhancement.
Hamartomas are habitually benign, but there is a
chance that they could become cancerous. Excision and histological examination
should be used to rule out the possibility of malignant transformation. For
example, in Cowden disease, which is a rare autosomal dominant disorder caused
by mutations in the PTEN onco-suppressor gene or related genes, there is an
increased risk of breast, thyroid, and endometrial neoplasia [1-4]. In the
clinical setting, hamartoma manifests as an asymptomatic mass or unilateral
breast enlargement without a palpable lump [1]. Some bilateral forms have been
described, and the onset of signs can vary from two months to two years [2].
Their mammographic appearance is that of ovoid masses
with a heterogeneous parenchymal density consistent with both soft tissue and
lipomatous elements, bordered by a thin radiolucent halo. Benign calcifications
can be visible. Even though large hamartomas can displace adjacent tissue and
show mild compression, they do not induce architectural distortion [5]. They
also show lobular densities inside the surrounding fat, giving them a
"slice of salami" appearance. In the presence of spiculated opacities
or pleomorphic calcifications, malignancy should be suspected [3]. On
ultrasound, they appear as well-circumscribed masses with a thin peripheral
capsule. They feature a heterogenous echotexture that includes both hypoechoic
and hyperechoic areas compared to the surrounding parenchyma. On colour
Doppler, they are usually avascular and have a firm consistency on
elastography. The degree of compressibility is proportional to the amount of
adipose tissue present and is also a feature of benign breast lesions [5].
When a mammogram shows a round mass with a radiolucent
halo and an ultrasound shows an oval, heterogeneous mass surrounded by an
echogenic or echo-lucent ring, hamartoma is confirmed [1]. On MRI, all of the
mass’s constituents can be discerned on various sequences, making them easy to
diagnose. This makes it an extremely useful imaging technique. They appear very
much like another breast within the breast (the breast within the breast sign).
Since both fat and soft tissues are present, they show mixed signal intensities
on T1WI and T2WI. Typically, the rim of pseudocapsules will be hypointense.
They exhibit a gradual and progressive enhancement with a type I kinetic curve
following dynamic post-contrast. The enhancement may be similar to that of
normal breast parenchyma. They do not show restriction on DWI, and ADC values
are high. Similar to the normal breast, spectroscopy will detect water and
lactate peaks along with a low choline level [5]. Core biopsy and US-guided
needle biopsy are unable to provide a diagnosis as there are no distinctive
features capable of characterizing the lesions. However, surgical removal can
identify the typical histological characteristics [4]. Usually, total excision
is the therapy of choice, but recurrence is seen in approximately 8% of cases
that have been reported [1].