首页 > 最新文献

Dermatology online journal最新文献

英文 中文
Reactive angioendotheliomatosis as a side effect of long-acting injectable insulin use. 反应性血管内皮瘤病作为长效注射胰岛素的副作用。
Q3 Medicine Pub Date : 2025-09-08 DOI: 10.25251/d8bxg891
Kennedy Stoll, Samantha Holmes Seward, Terrence M Katona, Sahand Rahnama-Moghadam

A 44-year-old woman with type II diabetes mellitus presented with an 8-month history of a painful, ulcerating rash at the area of insulin injection of her left lower abdomen. Topical antibiotics, topical corticosteroids, oral antibiotics, and supportive wound care provided no relief. A similar eruption developed on the right abdomen when she switched injection sites. Wedge biopsy of the violaceous, reticular plaque demonstrated a central dermal scar with surrounding lobular and linear collections of small blood vessels, consistent with reactive angioendotheliomatosis. This condition typically occurs secondary to an underlying systemic disease, but we believe hers was a side effect related to trauma from insulin injection or secondary to an insulin additive hypersensitivity. The patient was switched to a glucagon-like peptide-1 agonist, active lesions were treated with topical timolol 0.5% ophthalmic solution, and oral propranolol was started with upward titration. She continues to see improvement in pain and has not developed any new ulcerations at other sites on the body.

44岁2型糖尿病女性患者,左下腹胰岛素注射部位出现疼痛、溃疡性皮疹,病史8个月。局部抗生素、局部皮质类固醇、口服抗生素和支持性伤口护理均无缓解作用。当她更换注射部位时,右腹部也出现了类似的皮疹。紫色网状斑块的楔形活检显示中央真皮瘢痕,周围有小叶状和线状小血管聚集,与反应性血管内皮瘤病一致。这种情况通常继发于潜在的全身性疾病,但我们认为她的副作用与胰岛素注射创伤或继发于胰岛素添加剂过敏有关。患者改用胰高血糖素样肽-1激动剂,活动性病变局部给予0.5%的噻莫洛尔眼液治疗,开始口服普萘洛尔,剂量向上递增。她继续看到疼痛的改善,并没有在身体的其他部位发展任何新的溃疡。
{"title":"Reactive angioendotheliomatosis as a side effect of long-acting injectable insulin use.","authors":"Kennedy Stoll, Samantha Holmes Seward, Terrence M Katona, Sahand Rahnama-Moghadam","doi":"10.25251/d8bxg891","DOIUrl":"https://doi.org/10.25251/d8bxg891","url":null,"abstract":"<p><p>A 44-year-old woman with type II diabetes mellitus presented with an 8-month history of a painful, ulcerating rash at the area of insulin injection of her left lower abdomen. Topical antibiotics, topical corticosteroids, oral antibiotics, and supportive wound care provided no relief. A similar eruption developed on the right abdomen when she switched injection sites. Wedge biopsy of the violaceous, reticular plaque demonstrated a central dermal scar with surrounding lobular and linear collections of small blood vessels, consistent with reactive angioendotheliomatosis. This condition typically occurs secondary to an underlying systemic disease, but we believe hers was a side effect related to trauma from insulin injection or secondary to an insulin additive hypersensitivity. The patient was switched to a glucagon-like peptide-1 agonist, active lesions were treated with topical timolol 0.5% ophthalmic solution, and oral propranolol was started with upward titration. She continues to see improvement in pain and has not developed any new ulcerations at other sites on the body.</p>","PeriodicalId":11040,"journal":{"name":"Dermatology online journal","volume":"31 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421685","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bullous pemphigoid in a patient with immunoglobulin A nephropathy. 免疫球蛋白a肾病患者的大疱性类天疱疮。
Q3 Medicine Pub Date : 2025-09-08 DOI: 10.25251/ph1eq643
Alex Marti, Owen Dean, Brittney Schultz, Sara Hylwa

Bullous pemphigoid is a chronic autoimmune blistering disease typically presenting as non-specific pruritis following by the development of vesicles and bullae. A variety of medications and comorbid medical conditions have been associated with bullous pemphigoid. Herein, we present a case describing a potential novel association between immunoglobulin A nephropathy and bullous pemphigoid.

大疱性类天疱疮是一种慢性自身免疫性水疱疾病,典型表现为非特异性瘙痒,随后出现小泡和大疱。各种药物和合并症与大疱性类天疱疮有关。在此,我们提出一个病例描述免疫球蛋白a肾病和大疱性类天疱疮之间潜在的新联系。
{"title":"Bullous pemphigoid in a patient with immunoglobulin A nephropathy.","authors":"Alex Marti, Owen Dean, Brittney Schultz, Sara Hylwa","doi":"10.25251/ph1eq643","DOIUrl":"10.25251/ph1eq643","url":null,"abstract":"<p><p>Bullous pemphigoid is a chronic autoimmune blistering disease typically presenting as non-specific pruritis following by the development of vesicles and bullae. A variety of medications and comorbid medical conditions have been associated with bullous pemphigoid. Herein, we present a case describing a potential novel association between immunoglobulin A nephropathy and bullous pemphigoid.</p>","PeriodicalId":11040,"journal":{"name":"Dermatology online journal","volume":"31 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421543","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hidradenitis suppurativa-associated lymphedema: A case and review of the literature. 化脓性汗腺炎伴淋巴水肿1例及文献复习。
Q3 Medicine Pub Date : 2025-09-08 DOI: 10.25251/rhw51f12
Elnaz Pourgholi, Mahboobeh Freidoon, Sahar Dadkhahfar, Elham Keykha, Hojjat Layegh, Shirin Zaresharifi

Hidradenitis suppurativa is a chronic inflammatory skin disorder characterized by painful recurring pustules, nodules, abscesses, and sinus tract formation. Secondary lymphedema associated with hidradenitis suppurativa is an uncommon but severe condition, often resulting in significant morbidity. Although the exact link between lymphedema and chronic hidradenitis suppurativa is not fully understood, the chronic inflammatory process with scarring is a likely an important factor. Herein, we reported a 52-year-old man with untreated chronic hidradenitis suppurativa, nonalcoholic fatty liver disease-related cirrhosis, and secondary massive scrotal lymphedema, complicated by cellulitis and sepsis. Despite appropriate treatment, the patient's condition deteriorated and he unfortunately passed away two weeks after hospitalization. Additionally, we reviewed the literature on hidradenitis suppurativa-associated lymphedema, analyzing data from 51 patients. The majority were men with long-standing severe hidradenitis suppurativa. Surgical intervention was identified as the most commonly effective treatment modality, offering substantial improvements in function and appearance. However, some patients experienced postsurgery adverse events. In conclusion, this report highlights the importance of early detection and management of hidradenitis suppurativa and its complications to prevent patients' significant morbidity.

化脓性汗腺炎是一种慢性炎症性皮肤病,其特征是反复出现疼痛的脓疱、结节、脓肿和窦道形成。继发性淋巴水肿与化脓性汗腺炎是一种罕见但严重的疾病,通常导致显著的发病率。尽管淋巴水肿和慢性化脓性汗腺炎之间的确切联系尚不完全清楚,但慢性炎症过程伴瘢痕形成可能是一个重要因素。在此,我们报告了一名52岁男性,未经治疗的慢性化脓性汗腺炎,非酒精性脂肪性肝病相关肝硬化,继发性大量阴囊淋巴水肿,并发蜂窝组织炎和败血症。尽管接受了适当治疗,但病人病情恶化,不幸在住院两周后去世。此外,我们回顾了有关化脓性汗腺炎相关淋巴水肿的文献,分析了51例患者的数据。多数为长期严重化脓性汗腺炎的男性。手术干预被认为是最普遍有效的治疗方式,在功能和外观上提供了实质性的改善。然而,一些患者出现了术后不良事件。总之,本报告强调了早期发现和处理化脓性汗腺炎及其并发症的重要性,以防止患者的显著发病率。
{"title":"Hidradenitis suppurativa-associated lymphedema: A case and review of the literature.","authors":"Elnaz Pourgholi, Mahboobeh Freidoon, Sahar Dadkhahfar, Elham Keykha, Hojjat Layegh, Shirin Zaresharifi","doi":"10.25251/rhw51f12","DOIUrl":"10.25251/rhw51f12","url":null,"abstract":"<p><p>Hidradenitis suppurativa is a chronic inflammatory skin disorder characterized by painful recurring pustules, nodules, abscesses, and sinus tract formation. Secondary lymphedema associated with hidradenitis suppurativa is an uncommon but severe condition, often resulting in significant morbidity. Although the exact link between lymphedema and chronic hidradenitis suppurativa is not fully understood, the chronic inflammatory process with scarring is a likely an important factor. Herein, we reported a 52-year-old man with untreated chronic hidradenitis suppurativa, nonalcoholic fatty liver disease-related cirrhosis, and secondary massive scrotal lymphedema, complicated by cellulitis and sepsis. Despite appropriate treatment, the patient's condition deteriorated and he unfortunately passed away two weeks after hospitalization. Additionally, we reviewed the literature on hidradenitis suppurativa-associated lymphedema, analyzing data from 51 patients. The majority were men with long-standing severe hidradenitis suppurativa. Surgical intervention was identified as the most commonly effective treatment modality, offering substantial improvements in function and appearance. However, some patients experienced postsurgery adverse events. In conclusion, this report highlights the importance of early detection and management of hidradenitis suppurativa and its complications to prevent patients' significant morbidity.</p>","PeriodicalId":11040,"journal":{"name":"Dermatology online journal","volume":"31 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421610","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An unusual epithelial sheath neuroma in a 74-year-old woman. 74岁女性异常上皮鞘神经瘤。
Q3 Medicine Pub Date : 2025-09-08 DOI: 10.25251/sq4g4z85
Ava Tsapatsaris, Alejandro Gru

Epithelial sheath neuroma is a cutaneous tumor presenting as an erythematous and often painful lesion on the skin of the back. We report a 74-year-old woman with a 7mm epithelial sheath neuroma located on the right upper central back. The initial clinical impression was a basal cell carcinoma and histopathologically, the tumor mimicked a carcinoma with perineural invasion. She had no prior trauma or surgeries at the surgical site. She reported experiencing pain at the site of the tumor. Pain is a symptom of more than half of the reported epithelial sheath neuroma cases. The papule was excised, and there has been no recurrence at the surgical site. We report the unusual occurrence of this very uncommon neoplasm, a tumor that might be inadvertently confused with an aggressive squamous cell carcinoma.

上皮鞘神经瘤是一种皮肤肿瘤,表现为背部皮肤的红斑性病变,常伴有疼痛。我们报告了一位74岁的女性,在右侧上中央背部有一个7mm的上皮鞘神经瘤。最初的临床表现为基底细胞癌,组织病理学上,肿瘤类似于浸润神经周围的癌。她以前没有外伤或手术在手术部位。她报告说肿瘤部位疼痛。疼痛是超过一半的上皮鞘神经瘤病例的症状。丘疹已切除,手术部位无复发。我们报告这种罕见的肿瘤,它可能被误认为是侵袭性鳞状细胞癌。
{"title":"An unusual epithelial sheath neuroma in a 74-year-old woman.","authors":"Ava Tsapatsaris, Alejandro Gru","doi":"10.25251/sq4g4z85","DOIUrl":"https://doi.org/10.25251/sq4g4z85","url":null,"abstract":"<p><p>Epithelial sheath neuroma is a cutaneous tumor presenting as an erythematous and often painful lesion on the skin of the back. We report a 74-year-old woman with a 7mm epithelial sheath neuroma located on the right upper central back. The initial clinical impression was a basal cell carcinoma and histopathologically, the tumor mimicked a carcinoma with perineural invasion. She had no prior trauma or surgeries at the surgical site. She reported experiencing pain at the site of the tumor. Pain is a symptom of more than half of the reported epithelial sheath neuroma cases. The papule was excised, and there has been no recurrence at the surgical site. We report the unusual occurrence of this very uncommon neoplasm, a tumor that might be inadvertently confused with an aggressive squamous cell carcinoma.</p>","PeriodicalId":11040,"journal":{"name":"Dermatology online journal","volume":"31 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421606","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Generalized morphea profunda following COVID-19 messenger ribonucleic acid vaccination. COVID-19信使核糖核酸疫苗接种后的广泛性深度吗啡。
Q3 Medicine Pub Date : 2025-09-08 DOI: 10.25251/2qgerv78
Gillian C McPherson, Silas M Money, Adeline J Johnson, Loretta S Davis

Morphea is an uncommon inflammatory disorder characterized by progressive sclerosis of the skin and soft tissues. We describe the novel occurrence of generalized morphea profunda arising in close temporal association with the COVID-19 messenger ribonucleic acid vaccination series. An 80-year-old man presented with numerous areas of firm, tight skin across his trunk and extremities with associated itching and burning. He denied characteristic symptoms of systemic sclerosis. Physical examination revealed numerous indurated plaques, some with porcelain-white or sclerotic yellow centers, on the bilateral dorsal forearms, anterior waistline, and bilateral legs. There was no evidence of sclerodactyly or inflammatory arthritis. Punch biopsies showed thickened collagen bundles in the reticular dermis, diminished periadnexal fat, and a perivascular and interstitial mononuclear cell infiltrate. The hyalinizing fibrosing reaction extended into the fat and was manifested by notable expansion of the interlobular septa of the fat by dense collagen. He was started on oral methotrexate with significant improvement in symptoms and lesion induration at 14-month follow-up. This case report provides further insight into the potential dermatologic adverse events associated with COVID-19 messenger ribonucleic acid vaccination. Further investigation is needed to determine any predisposing patient-specific intrinsic factors, unrecognized pathophysiologic mechanisms, and approximate incidence of such adverse events.

多发性硬化是一种罕见的炎症性疾病,其特征是皮肤和软组织的进行性硬化。我们描述了与COVID-19信使核糖核酸疫苗系列密切相关的广泛性深斑的新发生。80岁男性,躯干和四肢多处皮肤紧绷,伴有瘙痒和灼烧。他否认有系统性硬化症的特征性症状。体格检查发现双侧前臂背侧、前腰线和双侧腿部有大量硬化斑块,部分中心呈瓷白色或硬化黄色。没有证据表明有指关节硬化或炎症性关节炎。穿刺活检显示网状真皮层胶原束增厚,附件周围脂肪减少,血管周围和间质单核细胞浸润。透明化纤维化反应延伸到脂肪中,表现为脂肪小叶间隔被致密的胶原蛋白明显扩张。他开始口服甲氨蝶呤,在14个月的随访中症状和病变硬化明显改善。本病例报告提供了与COVID-19信使核糖核酸疫苗接种相关的潜在皮肤不良事件的进一步见解。需要进一步的研究来确定任何易感的患者特异性内在因素,未被认识的病理生理机制,以及此类不良事件的大致发生率。
{"title":"Generalized morphea profunda following COVID-19 messenger ribonucleic acid vaccination.","authors":"Gillian C McPherson, Silas M Money, Adeline J Johnson, Loretta S Davis","doi":"10.25251/2qgerv78","DOIUrl":"https://doi.org/10.25251/2qgerv78","url":null,"abstract":"<p><p>Morphea is an uncommon inflammatory disorder characterized by progressive sclerosis of the skin and soft tissues. We describe the novel occurrence of generalized morphea profunda arising in close temporal association with the COVID-19 messenger ribonucleic acid vaccination series. An 80-year-old man presented with numerous areas of firm, tight skin across his trunk and extremities with associated itching and burning. He denied characteristic symptoms of systemic sclerosis. Physical examination revealed numerous indurated plaques, some with porcelain-white or sclerotic yellow centers, on the bilateral dorsal forearms, anterior waistline, and bilateral legs. There was no evidence of sclerodactyly or inflammatory arthritis. Punch biopsies showed thickened collagen bundles in the reticular dermis, diminished periadnexal fat, and a perivascular and interstitial mononuclear cell infiltrate. The hyalinizing fibrosing reaction extended into the fat and was manifested by notable expansion of the interlobular septa of the fat by dense collagen. He was started on oral methotrexate with significant improvement in symptoms and lesion induration at 14-month follow-up. This case report provides further insight into the potential dermatologic adverse events associated with COVID-19 messenger ribonucleic acid vaccination. Further investigation is needed to determine any predisposing patient-specific intrinsic factors, unrecognized pathophysiologic mechanisms, and approximate incidence of such adverse events.</p>","PeriodicalId":11040,"journal":{"name":"Dermatology online journal","volume":"31 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421513","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Higher socioeconomic status of practice location, urban setting, and mean office visit level of service are associated with higher skin closure costs. 较高的社会经济地位的诊所地点,城市环境和平均就诊服务水平与较高的皮肤闭合成本相关。
Q3 Medicine Pub Date : 2025-09-08 DOI: 10.25251/vtrz4w60
Brad R Woodie, Allison E Spraul, Justin A Freking, Kyle P Rismiller, Scott A Neltner, Alan B Fleischer

Excision of skin cancer may involve a closure that can substantially increase the total cost of care. Dermatologist-specific factors may predict closure billing. The objective was to identify characteristics that predict higher-than-expected closure costs following skin cancer excision. The study included general dermatologists who performed malignant excisions and closures in the 2022 United States Medicare population. K-means clustering was performed on each dermatologist's cost difference and their mean size of malignant excisions. Dermatologist characteristics were compared between clusters and effect sizes were calculated to ensure substantial magnitudes of difference. Compared with dermatologists in low-cost clusters, dermatologists in high-cost clusters had higher office visit levels of service (P<0.0001) and practiced in postal codes with higher household incomes (P<0.0001), lower social deprivation scores (P<0.0001), and more urban areas (P<0.0001). For only small excision sizes, the high-cost cluster had more female dermatologists (P<0.0001). General dermatologists who billed for office visits at higher levels or practiced in more urban and affluent areas had higher skin cancer excision closure costs. The dermatologist practice patterns described here may help inform strategies to reduce the cost of surgical care for skin cancer.

皮肤癌的切除可能涉及闭合,这可能大大增加护理的总费用。皮肤科医生特有的因素可以预测结案费用。目的是确定预测皮肤癌切除后高于预期的闭合成本的特征。该研究包括在2022年美国医疗保险人口中进行恶性切除和闭合的普通皮肤科医生。对每位皮肤科医生的成本差异及其恶性切除的平均大小进行k均值聚类。比较不同聚类之间的皮肤科医生特征,并计算效应大小以确保差异的显著程度。与低成本集群的皮肤科医生相比,高成本集群的皮肤科医生有更高的办公室就诊水平(P
{"title":"Higher socioeconomic status of practice location, urban setting, and mean office visit level of service are associated with higher skin closure costs.","authors":"Brad R Woodie, Allison E Spraul, Justin A Freking, Kyle P Rismiller, Scott A Neltner, Alan B Fleischer","doi":"10.25251/vtrz4w60","DOIUrl":"https://doi.org/10.25251/vtrz4w60","url":null,"abstract":"<p><p>Excision of skin cancer may involve a closure that can substantially increase the total cost of care. Dermatologist-specific factors may predict closure billing. The objective was to identify characteristics that predict higher-than-expected closure costs following skin cancer excision. The study included general dermatologists who performed malignant excisions and closures in the 2022 United States Medicare population. K-means clustering was performed on each dermatologist's cost difference and their mean size of malignant excisions. Dermatologist characteristics were compared between clusters and effect sizes were calculated to ensure substantial magnitudes of difference. Compared with dermatologists in low-cost clusters, dermatologists in high-cost clusters had higher office visit levels of service (P<0.0001) and practiced in postal codes with higher household incomes (P<0.0001), lower social deprivation scores (P<0.0001), and more urban areas (P<0.0001). For only small excision sizes, the high-cost cluster had more female dermatologists (P<0.0001). General dermatologists who billed for office visits at higher levels or practiced in more urban and affluent areas had higher skin cancer excision closure costs. The dermatologist practice patterns described here may help inform strategies to reduce the cost of surgical care for skin cancer.</p>","PeriodicalId":11040,"journal":{"name":"Dermatology online journal","volume":"31 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421555","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Primary cutaneous follicle center lymphoma presenting as frontal fibrosing alopecia. 原发性皮肤滤泡中心淋巴瘤表现为额部纤维化性脱发。
Q3 Medicine Pub Date : 2025-09-08 DOI: 10.25251/21edz034
Tiffany Liu, Michelle F Henry, Cynthia Magro

Primary cutaneous follicle center lymphoma rarely presents as macular alopecia and is typically characterized by solitary papules and nodules on the head, neck, and trunk. We report a 24-year-old woman with frontal alopecia that clinically resembled frontal fibrosing alopecia but was ultimately diagnosed as primary cutaneous follicle center lymphoma. The patient presented with pronounced alopecia over the left frontal scalp superimposed on milder bitemporal alopecia and intermittent symptoms of scalp irritation. Histopathologic examination of a scalp biopsy revealed a nodular lymphocytic infiltrate with irregular germinal centers localized to the adventitial dermis of the eccrine coil and the interadnexal interstitium. Immunophenotyping confirmed B-cell clonality, with findings consistent with primary cutaneous follicle center lymphoma. This case highlights the importance of biopsy in atypical alopecia presentations, as histologic findings were pivotal in diagnosing primary cutaneous follicle center lymphoma with concurrent frontal fibrosing alopecia features.

原发性皮肤毛囊中心性淋巴瘤很少表现为黄斑性脱发,通常表现为头部、颈部和躯干的孤立丘疹和结节。我们报告一位24岁女性额部脱发,临床表现与额部纤维化性脱发相似,但最终被诊断为原发性皮肤毛囊中心淋巴瘤。患者表现为左额部头皮明显脱发,并伴有轻度双颞部脱发和间歇性头皮刺激症状。头皮活检的组织病理学检查显示结节性淋巴细胞浸润,不规则的生发中心位于内分泌线圈的真皮外皮层和附件间质。免疫分型证实b细胞克隆,结果与原发性皮肤滤泡中心淋巴瘤一致。本病例强调了活检在非典型脱发表现中的重要性,因为组织学结果是诊断原发性皮肤毛囊中心淋巴瘤并发额叶纤维化性脱发特征的关键。
{"title":"Primary cutaneous follicle center lymphoma presenting as frontal fibrosing alopecia.","authors":"Tiffany Liu, Michelle F Henry, Cynthia Magro","doi":"10.25251/21edz034","DOIUrl":"10.25251/21edz034","url":null,"abstract":"<p><p>Primary cutaneous follicle center lymphoma rarely presents as macular alopecia and is typically characterized by solitary papules and nodules on the head, neck, and trunk. We report a 24-year-old woman with frontal alopecia that clinically resembled frontal fibrosing alopecia but was ultimately diagnosed as primary cutaneous follicle center lymphoma. The patient presented with pronounced alopecia over the left frontal scalp superimposed on milder bitemporal alopecia and intermittent symptoms of scalp irritation. Histopathologic examination of a scalp biopsy revealed a nodular lymphocytic infiltrate with irregular germinal centers localized to the adventitial dermis of the eccrine coil and the interadnexal interstitium. Immunophenotyping confirmed B-cell clonality, with findings consistent with primary cutaneous follicle center lymphoma. This case highlights the importance of biopsy in atypical alopecia presentations, as histologic findings were pivotal in diagnosing primary cutaneous follicle center lymphoma with concurrent frontal fibrosing alopecia features.</p>","PeriodicalId":11040,"journal":{"name":"Dermatology online journal","volume":"31 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421618","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A case of basal cell nevus syndrome with a SUFU mutation. 基底细胞痣综合征伴SUFU突变1例。
Q3 Medicine Pub Date : 2025-09-08 DOI: 10.25251/kqdbtw18
Joshua Aron, Mikel Muse, Blair Harris, Madison Reed, Jonathan Crane, Rene Bermudez

Basal cell nevus syndrome (Gorlin syndrome) is a rare genetic condition characterized by multiple basal cell carcinomas, often arising before age 20.  Most cases result from a mutation in the patched 1 gene-part of the sonic hedgehog pathway. Rarely, this condition is related to a suppressor of fused gene mutation, which occurs downstream from Smoothened, and is unresponsive to Smoothened inhibitors including vismodegib and sonidegib. Notably, basal cell nevus syndrome, secondary to a suppressor of fused gene mutation, is associated with a higher incidence of childhood medulloblastoma with implications for the patient and offspring.  A 72-year-old man with pearly papules coalescing into plaques across the nose and cheeks presented. The lesions had appeared as a teenager, and the patient reported his sister had similar lesions. Five biopsies, reviewed by three dermatopathologists, were consistent with basal cell carcinoma. Genetic testing was negative for patched 1 and patched 2 mutations but positive for a heterozygous suppressor of fused mutation. Patients with basal cell nevus syndrome should be treated with surgical excision, counseled on sun protection, screened and monitored for complications, and treated with vismodegib (if associated with patched 1 mutation) or itraconazole (if associated with suppressor of fused mutation).

基底细胞痣综合征(Gorlin综合征)是一种罕见的遗传性疾病,以多发性基底细胞癌为特征,通常发生在20岁之前。大多数病例是由1号补丁基因的突变引起的,这是sonic hedgehog通路的一部分。很少,这种情况与融合基因突变的抑制因子有关,发生在Smoothened下游,对Smoothened抑制剂(包括vismodegib和sonidegib)无反应。值得注意的是,继发于融合基因突变抑制因子的基底细胞痣综合征与儿童成神经管细胞瘤的高发病率相关,对患者和后代都有影响。72岁男性,鼻部及脸颊有珍珠丘疹合并成斑块。该病变在十几岁时就出现了,患者报告他的妹妹也有类似的病变。三名皮肤病理学家复查了五份活组织检查,结果与基底细胞癌一致。基因检测对1号和2号补丁突变呈阴性,而对融合突变的杂合抑制因子呈阳性。基底细胞痣综合征患者应手术切除治疗,建议防晒,筛查和监测并发症,并使用维莫替吉(如果与补丁1突变相关)或伊曲康唑(如果与融合突变抑制因子相关)治疗。
{"title":"A case of basal cell nevus syndrome with a SUFU mutation.","authors":"Joshua Aron, Mikel Muse, Blair Harris, Madison Reed, Jonathan Crane, Rene Bermudez","doi":"10.25251/kqdbtw18","DOIUrl":"https://doi.org/10.25251/kqdbtw18","url":null,"abstract":"<p><p>Basal cell nevus syndrome (Gorlin syndrome) is a rare genetic condition characterized by multiple basal cell carcinomas, often arising before age 20.  Most cases result from a mutation in the patched 1 gene-part of the sonic hedgehog pathway. Rarely, this condition is related to a suppressor of fused gene mutation, which occurs downstream from Smoothened, and is unresponsive to Smoothened inhibitors including vismodegib and sonidegib. Notably, basal cell nevus syndrome, secondary to a suppressor of fused gene mutation, is associated with a higher incidence of childhood medulloblastoma with implications for the patient and offspring.  A 72-year-old man with pearly papules coalescing into plaques across the nose and cheeks presented. The lesions had appeared as a teenager, and the patient reported his sister had similar lesions. Five biopsies, reviewed by three dermatopathologists, were consistent with basal cell carcinoma. Genetic testing was negative for patched 1 and patched 2 mutations but positive for a heterozygous suppressor of fused mutation. Patients with basal cell nevus syndrome should be treated with surgical excision, counseled on sun protection, screened and monitored for complications, and treated with vismodegib (if associated with patched 1 mutation) or itraconazole (if associated with suppressor of fused mutation).</p>","PeriodicalId":11040,"journal":{"name":"Dermatology online journal","volume":"31 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421443","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Longevity in dermatologists-why do so many dermatologists live so long? 皮肤科医生的长寿——为什么这么多皮肤科医生活得这么长?
Q3 Medicine Pub Date : 2025-09-08 DOI: 10.25251/30qqf945
Philip R Cohen, Jeffrey C Miller, Barbara A Burrall

Longevity refers to living a longer and healthier life than the average.  Many dermatologists are characterized by not only longevity, but also superaging.  The American Academy of Dermatology published the obituaries of 57 colleagues; 89% (51 of the 57 dermatologists) of the dermatologists were older than 80 years of age when they died.  It is remarkable that so many dermatologists live so long.  We propose that the longevity observed in dermatologists may not only be merely the result of chance.  We hypothesize that dermatologist longevity is the result of the genetic predisposition, lifestyle (such as healthy diets, exercise, and rest), and specific career characteristics.

长寿指的是比一般人活得更长、更健康。许多皮肤科医生的特点不仅是长寿,而且是超衰老。美国皮肤病学会(American Academy of Dermatology)发表了57位同事的讣告;89%(57名皮肤科医生中的51名)的皮肤科医生在死亡时年龄超过80岁。值得注意的是,这么多皮肤科医生活得这么久。我们认为,在皮肤科医生身上观察到的长寿可能不仅仅是偶然的结果。我们假设皮肤科医生的长寿是遗传倾向、生活方式(如健康饮食、锻炼和休息)和特定职业特征的结果。
{"title":"Longevity in dermatologists-why do so many dermatologists live so long?","authors":"Philip R Cohen, Jeffrey C Miller, Barbara A Burrall","doi":"10.25251/30qqf945","DOIUrl":"https://doi.org/10.25251/30qqf945","url":null,"abstract":"<p><p>Longevity refers to living a longer and healthier life than the average.  Many dermatologists are characterized by not only longevity, but also superaging.  The American Academy of Dermatology published the obituaries of 57 colleagues; 89% (51 of the 57 dermatologists) of the dermatologists were older than 80 years of age when they died.  It is remarkable that so many dermatologists live so long.  We propose that the longevity observed in dermatologists may not only be merely the result of chance.  We hypothesize that dermatologist longevity is the result of the genetic predisposition, lifestyle (such as healthy diets, exercise, and rest), and specific career characteristics.</p>","PeriodicalId":11040,"journal":{"name":"Dermatology online journal","volume":"31 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421572","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Utilizing artificial intelligence to address dermatology curriculum deficiencies in pre-clinical medical education. 利用人工智能解决临床前医学教育中皮肤病学课程的不足。
Q3 Medicine Pub Date : 2025-09-08 DOI: 10.25251/70k6fb79
Lauren McGrath, Melanie Rodriguez, Maria Mariencheck, Steven Feldman, Zeynep Akkurt

There are deficiencies in preclinical dermatology education: only 12% of medical schools in the United States offer a dedicated preclinical curriculum. Students could use free artificial intelligence as an alternative to other expensive resources to prepare for United States Medical Licensing Examination board examinations. ChatGPT was prompted to generate a dermatology curriculum including lecture outlines, disease pathology, histology, pharmacology, and practice questions based on the United States Medical Licensing Examination Step 1 content outline. The result was analyzed for completeness, accuracy, and quality. ChatGPT created a dermatology curriculum with 8 topics: introduction, infectious disorders, inflammatory disorders, neoplasms, integumentary disorders, pathology/histology, pharmacology, and clinical case studies. The curriculum included placeholders for the visual learning components rather than incorporating clinical images. The clinical vignettes included were incomplete and not detailed. Artificial intelligence can provide accessible, personalized, and cost-effective resources for preclinical medical students learning dermatology. This has the potential to impact inequalities among medical schools in dermatology education. However, generated curriculums need to be evaluated by dermatology educators to ensure accuracy and quality.

临床前皮肤科教育存在缺陷:美国只有12%的医学院提供专门的临床前课程。学生可以使用免费的人工智能来代替其他昂贵的资源来准备美国医疗执照考试委员会的考试。ChatGPT根据美国医师执照考试第1步的内容大纲,编写了一套皮肤病学课程,包括讲座大纲、疾病病理学、组织学、药理学和实践问题。分析结果的完整性、准确性和质量。ChatGPT创建了一个包含8个主题的皮肤病学课程:介绍,感染性疾病,炎症性疾病,肿瘤,表皮疾病,病理/组织学,药理学和临床病例研究。课程包括视觉学习部分的占位符,而不是纳入临床图像。包括的临床小插曲是不完整和不详细的。人工智能可以为临床前医学学生学习皮肤病学提供可访问的、个性化的和具有成本效益的资源。这有可能影响医学院在皮肤病学教育方面的不平等。然而,生成的课程需要由皮肤科教育者进行评估,以确保准确性和质量。
{"title":"Utilizing artificial intelligence to address dermatology curriculum deficiencies in pre-clinical medical education.","authors":"Lauren McGrath, Melanie Rodriguez, Maria Mariencheck, Steven Feldman, Zeynep Akkurt","doi":"10.25251/70k6fb79","DOIUrl":"https://doi.org/10.25251/70k6fb79","url":null,"abstract":"<p><p>There are deficiencies in preclinical dermatology education: only 12% of medical schools in the United States offer a dedicated preclinical curriculum. Students could use free artificial intelligence as an alternative to other expensive resources to prepare for United States Medical Licensing Examination board examinations. ChatGPT was prompted to generate a dermatology curriculum including lecture outlines, disease pathology, histology, pharmacology, and practice questions based on the United States Medical Licensing Examination Step 1 content outline. The result was analyzed for completeness, accuracy, and quality. ChatGPT created a dermatology curriculum with 8 topics: introduction, infectious disorders, inflammatory disorders, neoplasms, integumentary disorders, pathology/histology, pharmacology, and clinical case studies. The curriculum included placeholders for the visual learning components rather than incorporating clinical images. The clinical vignettes included were incomplete and not detailed. Artificial intelligence can provide accessible, personalized, and cost-effective resources for preclinical medical students learning dermatology. This has the potential to impact inequalities among medical schools in dermatology education. However, generated curriculums need to be evaluated by dermatology educators to ensure accuracy and quality.</p>","PeriodicalId":11040,"journal":{"name":"Dermatology online journal","volume":"31 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421623","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Dermatology online journal
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1