Erika Koh, Oluwadamilare Ajayi, Danielle McClanahan, Louise van der Weyden, Jamie Billington, Josephine IIott, David J Adams, Timothy McCalmont, Kevin White
{"title":"Congenital Adnexal Carcinoma with Cribriform Pattern in a Pediatric Patient.","authors":"Erika Koh, Oluwadamilare Ajayi, Danielle McClanahan, Louise van der Weyden, Jamie Billington, Josephine IIott, David J Adams, Timothy McCalmont, Kevin White","doi":"10.1097/DAD.0000000000003446","DOIUrl":"https://doi.org/10.1097/DAD.0000000000003446","url":null,"abstract":"<p><strong>Abstract: </strong>Primary cutaneous adnexal carcinomas are exceedingly rare in pediatric patients. A 12-year-old girl presented to the dermatology clinic with a congenital subcutaneous nodule on the left buttock. The patient underwent wide local excision, and histopathologic findings demonstrated large nodular aggregates of atypical basaloid cells with a sieve-like pattern. Immunohistochemical stains were positive for p63, AE1/AE3, β-catenin, and EMA. CK7, CK20, CD117, SOX-10, and Ber-Ep4 were negative. To the best of our knowledge upon review of the literature, we describe a new entity of an adnexal carcinoma with a cribriform pattern in a pediatric patient. Although there was no clinical evidence of recurrence at follow-up, the biologic potential of this tumor is unknown.</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":" ","pages":""},"PeriodicalIF":0.8,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149118322","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nasser Almadan, Reem Althubaiti, Ahmed Almotairi, Chibuzo Uguru, Abdullah AlBuqaey, Mahmoud AlAwa
{"title":"Dissecting a Diagnostic Enigma, Multiple Bilateral Facial Nodules in a Middle Aged Woman.","authors":"Nasser Almadan, Reem Althubaiti, Ahmed Almotairi, Chibuzo Uguru, Abdullah AlBuqaey, Mahmoud AlAwa","doi":"10.1097/DAD.0000000000003399","DOIUrl":"10.1097/DAD.0000000000003399","url":null,"abstract":"<p><strong>Abstract: </strong>Hereditary leiomyomatosis and renal cell carcinoma is a rare autosomal-dominant tumor predisposition syndrome that is caused by a germline defect in fumarate hydratase. We report a case of a 40-year-old woman who presented with multiple bilateral facial nodules arranged in a zosteriform pattern that increased in distribution over 15 years. The patient reported slight pain with eating spicy food and similar lesions in her younger sister. Biopsy was performed, and histopathological examination confirmed the diagnosis of pilar leiomyoma. An immunohistochemical study showed loss of fumarate hydratase in tumoral cells with a positive internal control, confirming the diagnosis of hereditary leiomyomatosis and renal cell carcinoma. An abdominal ultrasound was performed, revealing masses in the right and left ovaries and uterus, whereas the kidneys were free from masses. This case highlights the importance of clinical suspicion and histological evaluation for any bilateral facial nodules arranged in a zosteriform pattern, which can be part of a syndrome.</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":" ","pages":"810-814"},"PeriodicalIF":0.8,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148690211","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Lipomatosis of the Median Nerve: A Case Report.","authors":"Ayat N Ghazy, Eric C Honaker, Terrence M Katona","doi":"10.1097/DAD.0000000000003345","DOIUrl":"10.1097/DAD.0000000000003345","url":null,"abstract":"<p><strong>Abstract: </strong>Lipomatosis of nerve is a rare, nonhereditary congenital overgrowth disorder involving fibroadipose tissue proliferation along nerve territories, most commonly the median and plantar nerves. We report a case of a 35-year-old man presenting with slowly progressive enlargement of the thumb and index finger since childhood, associated with increasing discomfort. Imaging demonstrated nonencapsulated fatty overgrowth with digital nerve involvement and associated bony hypertrophy. Surgical management included right thumb debulking and distal phalanx amputation of the index finger. Histopathologic examination confirmed infiltration of epineural and perineurial structures by adipose and fibrous tissue, consistent with lipomatosis of the median nerve. Postoperatively, the patient exhibited diminished thumb sensation with a preserved range of motion. This case highlights the diagnostic role of imaging, along with radiologic-pathologic correlation and the potential for postoperative sensory loss because of unavoidable excision of involved nerve tissue.</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":" ","pages":"818-821"},"PeriodicalIF":0.8,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148334169","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Volha Lenskaya, Audrey Liu, Priyadharsini Nagarajan, Phyu P Aung, Jonathan L Curry, Carlos A Torres-Cabala
{"title":"Case Series of Cutaneous Rothia Mucilaginosa Infection and an Important Potential Pitfall Case.","authors":"Volha Lenskaya, Audrey Liu, Priyadharsini Nagarajan, Phyu P Aung, Jonathan L Curry, Carlos A Torres-Cabala","doi":"10.1097/DAD.0000000000003340","DOIUrl":"10.1097/DAD.0000000000003340","url":null,"abstract":"<p><strong>Abstract: </strong>Rothia mucilaginosa has emerged as an important opportunistic pathogen, challenging the traditional view of this organism as a harmless oral commensal. Invasive infections are increasingly recognized in immunocompromised patients, particularly those with hematolymphoid malignancies, solid organ, and stem cell transplants, and neutropenia. Cutaneous involvement, however, remains underrepresented and remains a diagnostic challenge in view of its ambiguous morphology in tissue sections and nonspecific special stains results. We report 3 cases of suspected or confirmed cutaneous involvement by R. mucilaginosa in immunocompromised patients with hematolymphoid malignancies and profound neutropenia. In all cases, the organisms appeared as small, round eosinophilic coccoid structures predominantly within the vascular spaces and forming aggregates within the papillary dermis. The organisms were positive on periodic acid-Schiff, Grocott methenamine silver, and gram stains, with some variable stain reactivity. One case demonstrated culture-proven R. mucilaginosa bacteremia with a fatal clinical course in the setting of systemic sepsis. In addition, we present a pitfall case in which platelet aggregates closely mimicked morphology of R. mucilaginosa aggregates, creating a potential diagnostic trap. In this context, CD61 immunohistochemistry was helpful in distinguishing platelet aggregates, which showed strong positivity, from R. mucilaginosa organisms, which were negative. Our findings highlight the importance of considering R. mucilaginosa in the differential diagnosis of cutaneous infections in immunocompromised patients and emphasize potential histopathologic pitfall. Awareness of the R. mucilaginosa morphologic features, its nonspecific findings on special stains and the use of adjunct immunohistochemical studies may help avoid misinterpretation and facilitate accurate diagnosis.</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":" ","pages":"786-790"},"PeriodicalIF":0.8,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148334241","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Carol Stegura, Nolan Steevens, Hannah Neimy, Shakthika Saravanan, Maya Andrade, Hannah Morgan, Luke Broughton, Kathryn Keller, Yousef Almutairi, Yingxue Huang, Tarik Al Nasseri, Mathew J Gregoski, Manuel Valdebran, Dirk Elston
{"title":"Assessing Nuclear and Nucleolar Areas Between Malignant Melanoma and Benign Nevi.","authors":"Carol Stegura, Nolan Steevens, Hannah Neimy, Shakthika Saravanan, Maya Andrade, Hannah Morgan, Luke Broughton, Kathryn Keller, Yousef Almutairi, Yingxue Huang, Tarik Al Nasseri, Mathew J Gregoski, Manuel Valdebran, Dirk Elston","doi":"10.1097/DAD.0000000000003355","DOIUrl":"10.1097/DAD.0000000000003355","url":null,"abstract":"<p><strong>Abstract: </strong>Distinguishing malignant melanoma (MM) from benign melanocytic nevi presents a diagnostic challenge that can result in suboptimal management. We sought to assess whether quantifying nuclear and nucleolar areas in histological samples provided utility in differentiation. Our study used deidentified hematoxylin and eosin (H&E)-stained teaching slides, 77 MM cases and 73 benign nevi cases (N = 150). Using ImageJ software, 20 nuclei and their corresponding nucleoli were measured per slide in square pixels and converted to square microns. Nuclei selection was contingent on visualization of the nuclear envelope and a singular nucleolus. Mann-Whitney U tests were applied to compare average nuclear and nucleolar areas between groups. Significant differences were observed in both nuclear and nucleolar areas. The mean nuclear area was significantly larger in MM compared with benign nevi (702.04 ± 236.55 μm 2 vs. 481.18 ± 153.89 μm 2 ; P < 0.001). Similarly, the mean nucleolar area was markedly larger in MM compared with benign nevi (90.88 ± 52.25 μm 2 vs. 58.03 ± 25.35 μm 2 ; P < 0.001).</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":" ","pages":"782-785"},"PeriodicalIF":0.8,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148267114","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hailey Fike, Shuai Li, Tessa Farnham, Andrew Siref
{"title":"Herpetic Whitlow in Association With a Cutaneous Infiltrate of Chronic Lymphocytic Leukemia.","authors":"Hailey Fike, Shuai Li, Tessa Farnham, Andrew Siref","doi":"10.1097/DAD.0000000000003357","DOIUrl":"10.1097/DAD.0000000000003357","url":null,"abstract":"","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":" ","pages":"815-817"},"PeriodicalIF":0.8,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148363808","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ana L Toussaint, Carlos Sánchez-Cárdenas, Ruth Fuentes-García, Yann Charli-Joseph, Sonia Toussaint-Caire
{"title":"PRAME Immunostaining in Acral Melanocytic Proliferations: A Meta-Analysis.","authors":"Ana L Toussaint, Carlos Sánchez-Cárdenas, Ruth Fuentes-García, Yann Charli-Joseph, Sonia Toussaint-Caire","doi":"10.1097/DAD.0000000000003299","DOIUrl":"10.1097/DAD.0000000000003299","url":null,"abstract":"<p><strong>Abstract: </strong>Acral cutaneous melanoma is a highly aggressive form of skin cancer that develops in palms, soles, and/or the nail unit. PReferentially expressed Antigen in MElanoma (PRAME) is an immunohistochemical marker that has shown a high degree of expression in cutaneous melanomas. However, no meta-analysis has previously focused on acral melanocytic proliferations. Herein, we performed the first meta-analysis to objectify the utility of PRAME immunohistochemistry, focusing on this understudied subtype of melanocytic proliferations involving acral sites. Thirteen studies were identified, which included 930 lesions (557 malignant and 373 benign). A random-effects model was used to calculate sensitivity, specificity, and likelihood ratios. Summary receiver operating characteristic curves and forest plots were created, and heterogeneity was assessed using Cochran Q and I 2 statistics. PRAME expression in acral melanoma showed the highest diagnostic accuracy at a cutoff value of 3+/50%, pertaining to the optimal balance between sensitivity and specificity (78% and 92%, respectively). Although PRAME immunostaining enhances the accurate diagnosis of acral melanocytic proliferations, its expression in atypical and borderline melanocytic proliferations remains controversial and shows considerable variability. Thus, the definitive diagnosis of acral melanoma still relies on careful clinicopathologic assessment and, occasionally, molecular correlation.</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":" ","pages":"775-781"},"PeriodicalIF":0.8,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148334286","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Demonstration of 23-Gene Expression Profile Test Utility Within PRAME Immunohistochemistry Results: A Case Series.","authors":"Gregory A Hosler, Matthew S Goldberg, Etan Marks","doi":"10.1097/DAD.0000000000003365","DOIUrl":"10.1097/DAD.0000000000003365","url":null,"abstract":"<p><strong>Abstract: </strong>Histopathological examination using hematoxylin and eosin (H&E)-stained tissue is sufficient for diagnosing most melanocytic neoplasms as benign or malignant; however, diagnostic tools such as PRAME (preferentially expressed antigen in melanoma) immunohistochemistry (IHC) and the 23-gene expression profile (23-GEP) test can aid in the analysis of histopathologically ambiguous lesions, which can be referred to as diagnostically challenging, equivocal, indeterminate, or uncertain. When compared with the gold standard of H&E diagnosis by a dermatopathologist, PRAME IHC showed 83.2% sensitivity and 99.3% specificity in an initial validation cohort and 23-GEP showed 91.5% sensitivity and 92.7% specificity in an independent validation cohort. In addition, 23-GEP has been evaluated in 3 studies with patients with known outcomes (eg, metastasis) and has reported metrics of 90.4%-96.3% sensitivity and 87.3%-96.2% specificity in distinguishing benign versus malignant melanocytic neoplasms. In this study, we present the utility of the 23-GEP test within 8 equivocal cases with various PRAME IHC staining patterns. Cases underwent histopathological review and received at least 4 and up to 5 diagnoses each. In samples where PRAME IHC is inconclusive, conflicting, or ambiguous regarding a final diagnosis, the 23-GEP can provide additional diagnostic information to upgrade or downgrade the overall malignant potential of the lesion in question.</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":" ","pages":"791-797"},"PeriodicalIF":0.8,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13585158/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148334225","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A Look Back at Mercury Soap as a Treatment for Yaws.","authors":"John A Papalas","doi":"10.1097/DAD.0000000000003364","DOIUrl":"https://doi.org/10.1097/DAD.0000000000003364","url":null,"abstract":"<p><strong>Abstract: </strong>The centuries-old practice of using mercury as a treatment for syphilis is well-known. The historical use of mercury for other treponematoses is less well-recognized. Afridol was a mercury containing soap produced by Bayer which they promoted as a cure for various cutaneous aliments, including yaws (frambosia). In this article, I briefly outline the development of Afridol and its subsequent marketing with the use of early 20th century medical advertising art.</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":"48 10","pages":"770-774"},"PeriodicalIF":0.8,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149002854","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}