Clinical and histopathologic differentiation between early acral melanoma and acral nevus is often difficult. Dermoscopy is helpful in this differentiation. On dermoscopy, early acral melanoma shows the parallel ridge pattern showing band-like pigmentation on the ridges of the surface skin markings, whereas a representative dermoscopic pattern in acquired acral nevus is the parallel furrow pattern showing parallel linear pigmentation along the surface furrows. The parallel furrow pattern suggests that melanocytes of acral nevus preferentially proliferate in the crista profunda limitans, an epidermal rete ridge underlying the surface furrow. In the present study, however, we found that in 13 of 18 acquired acral nevi, proliferation of melanocytes were detected not only in the crista profunda limitans but also in the crista profunda intermedia (CPI), an epidermal rete ridge underlying the surface ridge. Very interestingly, Fontana-Masson staining of these acral nevi revealed that even when proliferation of melanocytes was prominent in the CPI, melanin granules in the cornified layer were observed as regular melanin columns situated under the surface furrows and were hardly detected under the surface ridges. These findings indicate that in acral nevus, melanin granules produced by melanocytes in the CPI are not transferred to the upper epidermis. Hence, we must be careful not to overdiagnose an acral melanocytic lesion in which an increased number of melanocytes are detected in the CPI. Even in such a case, if melanin granules in the cornified layer are detected as melanin columns regularly distributed under the surface furrows, the lesion is strongly suggested to be a benign acral nevus.
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http://dx.doi.org/10.1097/DAD.0b013e318201ac8f | DOI Listing |
Diagn Pathol
December 2024
Department of Pathology, Hospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, 210042, China.
Background: Isolated immunohistochemical indicators are limited to diagnose melanocytic neoplasms. This retrospective study is to assess the diagnostic value of combined immunohistochemical analysis targeting preferentially expressed antigen in melanoma (PRAME) and p16 in melanocytic neoplasms, with a detailed focus on arcal lesions.
Methods: This was a single center cohort study from January 2022 to June 2023.
J Am Acad Dermatol
November 2024
Department of Oncology, Cancer Center, The First Hospital of Jilin University, Changchun, China. Electronic address:
Background: It is unknown whether acral melanomas (AMs) associated with pre-existing nevi have similar risk to other AMs.
Objective: To compare risk of recurrence and death between AMs associated with pre-existing nevi and de novo AMs.
Methods: We conducted a multicenter retrospective cohort study involving patients diagnosed with AMs between February 2011 and November 2022.
Dermatology
December 2024
First Department of Dermatology, School of Medicine, Aristotle University, Thessaloniki, Greece.
J Cutan Pathol
October 2024
Department of Pathology, University of Rochester Medical Center, Rochester, New York, USA.
Med Biol Eng Comput
November 2024
Department of Electronics and Communication Engineering, Mahatma Gandhi Institute of Technology, Gandipet, Hyderabad, India.
Melanoma is an uncommon and dangerous type of skin cancer. Dermoscopic imaging aids skilled dermatologists in detection, yet the nuances between melanoma and non-melanoma conditions complicate diagnosis. Early identification of melanoma is vital for successful treatment, but manual diagnosis is time-consuming and requires a dermatologist with training.
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