Sir: The use of ultrasound “on the surface” was hypothesized by Scuderi et al. in 19871 and resumed by Zocchi in 1996.2 Ultrasound-assisted liposuction is as a technique that can be associated with suction- assisted lipectomy.3 This new technique is called external ultrasound-assisted lipectomy. Whereas ultrasound-assisted liposuction emulsifies adipose tissue due to adipocyte membrane lysis, external ultrasound-assisted lipectomy, being less “invasive,” induces cell-to-cell contact loss and alters collagenic fibers. This leads to an easier detachment of adipose cells, which remain unaltered and can be mechanically removed. The external ultrasound-assisted lipectomy technique is the transcutaneous application of ultrasound by means of high-frequency ultrasound upon massive infiltrated tissue, followed by traditional liposuction. Results showed that several different effects were detected on both adipocytes and collagen fibers. In fact, patients treated with a 1-MHz frequency and a potency of 3 W showed no cell destruction, and collagenic fibers were partly conglomerated. In particular, using standard histological methods, it was difficult to distinguish between artifacts, detectable in both treated and control samples, and putative ultrasound destruction. Oil red-O staining, performed on cryosections, is capable of avoiding artifacts and confirmed that in only a small quantity of cases did adipocytes present with rounded membranes, and in limited cases, cells were detached from one another. In fact, immunofluorescence showed that these fibers were either intact or conglomerated, when the ultrasound frequency was 1 MHz (Fig. 1).Fig. 1.: Abdominal adipose biopsy from a patient treated with 1 MHz. Immunofluorescence phycoerythrin staining for collagen type I fibers showed that they had a normal appearance (original magnification ×200).In contrast, when the ultrasound frequencies were 2 and 3 MHz with a potency of 3 W, adipocyte alterations were observed. The latter was confirmed using the oil red-O stain, showing complete derangement of fat tissue occurring in biopsies of 3-Mhz-treated patients. In addition, a diffuse collagen fiber retraction, as shown at the immunofluorescence level (Fig. 2), was observed. This was particularly evident when comparing the biopsies of intact controls, which showed normal adipose tissue and intact collagen fibers.Fig. 2.: Abdominal adipose biopsy belonging to a patient treated with a frequency of 3 MHz. Immunofluorescence phycoerythrin staining for collagen type I fibers showed that they were completely retracted (original magnification ×200).External ultrasound-assisted lipectomy is a good method for the removal of localized fat in patients with moderate obesity.4 Few studies have been performed up to now with regard to the effects of external ultrasound-assisted lipectomy on adipose cells. A previous study5 focused on adipose and breast tissue, but it did not take into consideration that adipose cells are subjected to many histological artifacts. In addition, no observations were made of collagen fibers. This is rather important when using external ultrasound-assisted lipectomy, because fat tissue derangement may involve the whole architecture and, primarily, collagen. In conclusion, we have assessed that when using a frequency of 1 MHz, no alterations or only limited adipocytic alterations are observed, which do not include collagen fibers. Therefore, the technique can be used in aesthetic medicine (localized lipodystrophy, first-degree PEFS), using these frequencies. Both the 2- and 3-MHz frequencies are able to lead to complete fat tissue disruption, including adipose cells and collagenic fibers and can be indicated for fibrous and inveterate cellulitis (second and third- degree PEFS), in body contouring surgery. Francesco D’Andrea, M.D. Giuseppe A. Ferraro, M.D. Gian Franco Nicoletti, M.D. Dipartimento di Scienze Ortopediche, Traumatologiche, Riabilitative e Plastico-Ricostruttive Francesco De Francesco, M.D. Dipartimento di Medicina Sperimentale Sezione di Istologia ed Embriologia TESLAB Seconda Università di Napoli Napoli, Italy