References
- Huilgol SC, Ramnarain N, Carrington P, Leigh IM, Black MM. Cytokeratins in primary cutaneous amyloidosis. Australas J Dermatol. 1998;39(2):81–85. doi:https://doi.org/10.1111/j.1440-0960.1998.tb01253.x.
- Hashimoto K. 1984. Progress on cutaneous amyloidoses. J Invest Dermatol. 82(1):1–3. doi:https://doi.org/10.1111/1523-1747.ep12258661
- Mehrotra K, Dewan R, Kumar JV, Dewan A. Primary Cutaneous Amyloidosis: a Clinical, Histopathological and Immunofluorescence Study. J Clin Diagn Res. 2017;11(8):Wc01–wc05. doi:https://doi.org/10.7860/jcdr/2017/24273.10334.
- Weidner T, Illing T, Elsner P. 2017. Primary Localized Cutaneous Amyloidosis: a Systematic Treatment Review. Am J Clin Dermatol. 18(5):629–42. doi:https://doi.org/10.1007/s40257-017-0278-9
- Esmat SM, Fawzi MM, Gawdat HI, Ali HS, Sayed SS. Efficacy of different modes of fractional CO2 laser in the treatment of primary cutaneous amyloidosis: a randomized clinical trial. Lasers Surg Med. 2015;47(5):388–95. doi:https://doi.org/10.1002/lsm.22361.
- Norisugi O, Yamakoshi T, Shimizu T. 2014. Successful treatment of lichen amyloidosis using a CO2 surgical laser. Dermatol Ther. 27(2):71–73. doi:https://doi.org/10.1111/dth.12057
- Panchaprateep R, Tusgate S, Munavalli GS, Noppakun N. Fractional 1,550nm Ytterbium/Erbium fiber laser in the treatment of lichen amyloidosis: clinical and histological study. Lasers Surg Med. 2015;47(3):222–30. doi:https://doi.org/10.1002/lsm.22338.
- Ostovari N, Mohtasham N, Oadras MS, Malekzad F. 532-nm and 1064-nm Q-switched Nd:YAG laser therapy for reduction of pigmentation in macular amyloidosis patches. J Eur Acad Dermatol Venereol. 2008;22(4):442–46. doi:https://doi.org/10.1111/j.1468-3083.2007.02473.x.
- Liu H-T. 2000. Treatment of lichen amyloidosis (LA) and disseminated superficial porokeratosis (DSP) with frequency-doubled Q-switched Nd:YAG laser. Dermatol Surg. 26(10):958–62. doi:https://doi.org/10.1046/j.1524-4725.2000.026010958.x
- Khurana N, Urman C.The Efficacy of Q-Switched ND:YAG 1064 nm Laser in Recalcitrant Macular Amyloidosis: a Case Report. J Drugs Dermatol. 2016;15(11):1456–58.
- Barsky M, Buka RL.Pulsed dye laser for the treatment of macular amyloidosis: a case report. Cutis. 2014;93(4):189–92.
- Sawamura D, Sato-Matsumura KC, Shibaki A, Akiyama M, Kikuchi T, Shimizu H. A case of lichen amyloidosis treated with pulsed dye laser. J Eur Acad Dermatol Venereol. 2005;19(2):262–63. doi:https://doi.org/10.1111/j.1468-3083.2005.01038.x.
- Radmanesh M, Ghanatir F, Radmanesh R. Comparing the efficacy of pulsed dye laser, Q-Switched Nd-YAG, CO2, and combined CO(2) and Q-Switched Nd-YAG lasers for the treatment of cutaneous macular amyloidosis. J Dermatolog Treat. 2019;1–3. doi:https://doi.org/10.1080/09546634.2019.1654071.
- Torbeck RL, Schilling L, Khorasani H, Dover JS, Arndt KA, Saedi N. Evolution of the Picosecond Laser: a Review of Literature. Dermatol Surg. 2019;45(2):183–94. doi:https://doi.org/10.1097/dss.0000000000001697.
- Anderson RR, Margolis RJ, Watenabe S, Flotte T, Hruza GJ, Dover JS. Selective photothermolysis of cutaneous pigmentation by Q-switched Nd: YAG laser pulses at 1064, 532, and 355 nm. J Invest Dermatol. 1989;93(1):28–32. doi:https://doi.org/10.1111/1523-1747.ep12277339.
- Kopera D, Hohenleutner U, Stolz W, Landthaler M. Ex vivo quality-switched ruby laser irradiation of cutaneous melanocytic lesions: persistence of S-100-, HMB-45- and Masson-positive cells. Dermatology. 1997;194(4):344–50. doi:https://doi.org/10.1159/000246133.
- Kim JH, Kim H, Park HC, Kim IH. Subcellular selective photothermolysis of melanosomes in adult zebrafish skin following 1064-nm Q-switched Nd:YAG laser irradiation. J Invest Dermatol. 2010;130(9):2333–35. doi:https://doi.org/10.1038/jid.2010.129.
- Mun JY, Jeong SY, Kim JH, Han SS, Kim IH. A low fluence Q-switched Nd:YAG laser modifies the 3D structure of melanocyte and ultrastructure of melanosome by subcellular-selective photothermolysis. J Electron Microsc (Tokyo). 2011;60(1):11–18. doi:https://doi.org/10.1093/jmicro/dfq068.
- Picosecond Laser KK. 2017. Treatment for tattoos and benign cutaneous pigmented lesions (Secondary publication). Laser Ther. 26(4):274–81. doi:https://doi.org/10.5978/islsm.17-RE-02
- Negishi K, Akita H, Matsunaga Y. 2018. Prospective study of removing solar lentigines in Asians using a novel dual-wavelength and dual-pulse width picosecond laser. Lasers Surg Med. 50(8):851–58. doi:https://doi.org/10.1002/lsm.22820
- Brownstein MH, Helwig EB.The cutaneous amyloidoses. I. Localized forms. Arch Dermatol. 1970;102(1):8–19.doi:https://doi.org/10.1001/archderm.1970.04000070010002.
- Hoang Viet M, Derreumaux P, Li MS, Roland C, Sagui C, Nguyen PH. Picosecond dissociation of amyloid fibrils with infrared laser: a nonequilibrium simulation study. J Chem Phys. 2015;143(15):155101. doi:https://doi.org/10.1063/1.4933207.
- Kawasaki T, Yaji T, Ohta T, Tsukiyama K, Nakamura K. Dissociation of β-Sheet Stacking of Amyloid β Fibrils by Irradiation of Intense, Short-Pulsed Mid-infrared Laser. Cell Mol Neurobiol. 2018;38(5):1039–49. doi:https://doi.org/10.1007/s10571-018-0575-8.
- Kawasaki T, Fujioka J, Imai T, Torigoe K, Tsukiyama K. Mid-infrared free-electron laser tuned to the amide I band for converting insoluble amyloid-like protein fibrils into the soluble monomeric form. Lasers Med Sci. 2014;29(5):1701–07. doi:https://doi.org/10.1007/s10103-014-1577-5.
- Maddison B, Namazi MR, Samuel LS, Sanchez J, Pichardo R, Stocks J, Maruziva D, Yosipovitch G. Unexpected diminished innervation of epidermis and dermoepidermal junction in lichen amyloidosus. Br J Dermatol. 2008;159(2):403–06. doi:https://doi.org/10.1111/j.1365-2133.2008.08685.x.
- Esmat SM, Fawzi MM, Gawdat HI, Ali HS, Sayed SS. Efficacy of different modes of fractional CO2 laser in the treatment of primary cutaneous amyloidosis: a randomized clinical trial. Lasers Surg Med. 2015;47(5):388–95. doi:https://doi.org/10.1002/lsm.22361.