Re: Expanding dermatologic ultrasonography applications: further insights for enhanced patient management
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I read with great interest the recently published letter to the editor by Dr. Mese [1], and I agree that the applications of dermatologic ultrasound have grown exponentially during the last decade, as also mentioned in our article that was recently published in Ultrasonography [2].
As Dr. Mese pointed out, there are numerous applications in what is called "soft tissues ultrasonography" that can extend beyond dermatology. Although we were not able to fully address these applications in our article due to space restrictions; multiple publications and books have extensively discussed them [2-7].
I would like to make a few comments on the ultrasonographic descriptions presented by Dr. Mese [1]. One of them relates to the ultrasonographic appearance of lipomas, because this depends on the type of tissues mixed with the fat. If the lipoma is intermixed with fibrous tissue, it is called fibrolipoma, which usually appears as an oval, well-defined, hypoechoic, hypodermal structure that tends to follow the axis of the skin layers. If capillary vessels are present throughout the fat, it is called angiolipoma, which tends to manifest as a round or oval hyperechoic structure [5,7]. Posterior acoustic enhancement is not prominent in these structures compared to cystic lesions, and they usually do not generate a posterior acoustic enhancement artifact [8,9].
The ultrasonographic appearance of foreign bodies depends on their organic or inert nature; both of these usually present as linear hyperechoic structures, but inert foreign bodies such as metal or glass generate a posterior acoustic reverberation. Hypoechoic tissue in the periphery of a foreign body due to inflammation and granulomatous tissue is commonly seen [5,7].
One of the most prominent characteristics of warts is the fusiform shape, which accompanies their hypoechoic epidermal and dermal structure [4,5,7].
Regarding cutaneous psoriasis, epidermal thickening and undulation are frequently present, as well as dermal hypoechogenicity due to inflammation. In my experience and as far as I know, the literature contains no reports of dermal hyperechogenicity in psoriasis. Furthermore, dermal echogenicity is inverted under inflammation and frequently transitions from normal hyperechogenicity to a hypoechoic inflamed stage [5,7,10].
Last but not least, I would like to deeply thank Dr. Mese for bringing valuable information to the discussion.
Notes
No potential conflict of interest relevant to this article was reported.