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Annals of dermatology最新文献

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Insulin-Derived Cutaneous Amyloidosis: A Possible Complication of Repeated Insulin Injections. 胰岛素源性皮肤淀粉样变性：重复胰岛素注射的可能并发症。
Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.20.207
Hyeon Jeong Park, Won-Serk Kim, Seung-Wan Chae, Young-Jun Choi
{"title":"Insulin-Derived Cutaneous Amyloidosis: A Possible Complication of Repeated Insulin Injections.","authors":"Hyeon Jeong Park,&nbsp;Won-Serk Kim,&nbsp;Seung-Wan Chae,&nbsp;Young-Jun Choi","doi":"10.5021/ad.20.207","DOIUrl":"10.5021/ad.20.207","url":null,"abstract":"<p><p>Primary localized cutaneous amyloidosis (PLCA) is characterized by extracellular deposition of pathological fibril aggregation of proteins in the skin without systemic involvement. Macular amyloidosis, lichen (papular) amyloidosis, and nodular amyloidosis are three different subtypes of PLCA. Although the pathological mechanism of PLCA has not yet been clarified, it is assumed that a nucleus formation of amyloid fibril is formed due to repeated external stimulation, such as subcutaneous injection, which often poses diagnostic challenges. Herein, we present a 54-year-old Korean male patient with cutaneous localized amyloidosis which occurred after repeated local insulin injections, and discuss the relationship between insulin therapy in patients with diabetes mellitus and dermal amyloid deposition.</p>","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S71-S75"},"PeriodicalIF":0.0,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/ee/b6/ad-35-S71.PMC10608354.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49687065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Refractory Epidermolysis Bullosa Acquisita with Chronic Graft-versus-Host Disease Successfully Treated with Rituximab. 利妥昔单抗成功治疗难治性大疱性痤疮表皮松解症伴慢性移植物抗宿主病。
Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.20.332
Ju Hee Han, Hwa Jung Yook, Chul Hwan Bang, Ji Hyun Lee, Young Min Park, Jun Young Lee
{"title":"Refractory Epidermolysis Bullosa Acquisita with Chronic Graft-versus-Host Disease Successfully Treated with Rituximab.","authors":"Ju Hee Han,&nbsp;Hwa Jung Yook,&nbsp;Chul Hwan Bang,&nbsp;Ji Hyun Lee,&nbsp;Young Min Park,&nbsp;Jun Young Lee","doi":"10.5021/ad.20.332","DOIUrl":"10.5021/ad.20.332","url":null,"abstract":"","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S129-S131"},"PeriodicalIF":0.0,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/fe/4e/ad-35-S129.PMC10608369.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49687075","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Successful Treatment of Recalcitrant Palmoplantar Pustulosis with Guselkumab. Guselkumab成功治疗顽固性掌跖Pustulosis。
Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21b.064
Jang Hwan Jung, Sun Mun Jeong, Do Ik Kwon, Seol Hwa Seong, Joon Hee Kim, Jong Bin Park, Kee Suck Suh, Min Soo Jang
{"title":"Successful Treatment of Recalcitrant Palmoplantar Pustulosis with Guselkumab.","authors":"Jang Hwan Jung,&nbsp;Sun Mun Jeong,&nbsp;Do Ik Kwon,&nbsp;Seol Hwa Seong,&nbsp;Joon Hee Kim,&nbsp;Jong Bin Park,&nbsp;Kee Suck Suh,&nbsp;Min Soo Jang","doi":"10.5021/ad.21b.064","DOIUrl":"10.5021/ad.21b.064","url":null,"abstract":"Palmoplantar","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S165-S167"},"PeriodicalIF":0.0,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/98/83/ad-35-S165.PMC10608383.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49687081","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
A Case of Palisaded Neutrophilic and Granulomatous Dermatitis Associated with an Initial Presentation in Ankylosing Spondylitis. 一例与强直性脊柱炎初始表现相关的中性粒细胞和肉芽肿性皮炎。
Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21.063
Young Sun Suh, Eui Chang Jung, Yun Sun Moon, Seung-Geun Lee, Hyun-Ok Kim
{"title":"A Case of Palisaded Neutrophilic and Granulomatous Dermatitis Associated with an Initial Presentation in Ankylosing Spondylitis.","authors":"Young Sun Suh,&nbsp;Eui Chang Jung,&nbsp;Yun Sun Moon,&nbsp;Seung-Geun Lee,&nbsp;Hyun-Ok Kim","doi":"10.5021/ad.21.063","DOIUrl":"10.5021/ad.21.063","url":null,"abstract":"<p><p>Palisaded neutrophilic and granulomatous dermatitis (PNGD) is an inflammatory dermatosis associated with systemic immune-mediated diseases such as rheumatoid arthritis, systemic sclerosis, lupus erythematosus, and ulcerative colitis. Histologically, serial development of leukocytoclastic vasculitis is shown from an early stage, which can progress to palisading granuloma in the fully developed stage and to fibrosis in the final stage. A 32-year-old man presented with ankylosing spondylitis showing multiple erythematous papules on his fingers, elbows, knees, and left auricle. Histologic examination from his skin lesion revealed a perforating palisading granuloma with leukocytoclastic vasculitis, which was consistent with PNGD. Therefore, this study reported a case of PNGD accompanied by ankylosing spondylitis as an initial presentation.</p>","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S34-S37"},"PeriodicalIF":0.0,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/17/11/ad-35-S34.PMC10608376.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49686948","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
A Case of Perineal Hemangioma, External Genitalia Malformations, Lipomyelomeningocele, Vesicorenal Abnormalities, Imperforate Anus, and Skin Tag (PELVIS) Syndrome with Extensive Perineal Infantile Hemangioma. 1例伴广泛性腓婴儿血管瘤的腓血管瘤、外生殖器畸形、骨髓脊膜膨出、膀胱肾异常、肛门闭锁和皮肤标签（PELVIS）综合征。
Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21.183
Hye Won Hwang, Seon Bok Lee, Jeonghyun Shin, Gwang Seong Choi, Ji Won Byun
{"title":"A Case of Perineal Hemangioma, External Genitalia Malformations, Lipomyelomeningocele, Vesicorenal Abnormalities, Imperforate Anus, and Skin Tag (PELVIS) Syndrome with Extensive Perineal Infantile Hemangioma.","authors":"Hye Won Hwang,&nbsp;Seon Bok Lee,&nbsp;Jeonghyun Shin,&nbsp;Gwang Seong Choi,&nbsp;Ji Won Byun","doi":"10.5021/ad.21.183","DOIUrl":"10.5021/ad.21.183","url":null,"abstract":"<p><p>PELVIS syndrome describes the constellation of perineal hemangioma, external genitalia malformations, lipomyelomeningocele, vesicorenal abnormalities, imperforate anus, and skin tag. A 2-month-old girl presented with infantile hemangioma on her perineum and genitalia with imperforate anus, rectovaginal fistula and perineal skin tag at birth. Under the impression of PELVIS syndrome, consequential spinal sonography was conducted and revealed an intrasacral meningocele without clinical neurologic deficit. The anorectal malformation was surgically corrected, she was taking oral propranolol for the cutaneous lesion, and she showed improvement and no complications.</p>","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S88-S92"},"PeriodicalIF":0.0,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/34/38/ad-35-S88.PMC10608397.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49686949","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Superficial CD34-Positive Fibroblastic Tumor: Two Case Reports. 表面CD34阳性成纤维细胞瘤2例报告。
Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.20.328
Jung Eun Yim, Hyeong Mok Kwon, Hye Ri Kim, Dong Hoon Shin, Jong Soo Choi, Joon Hyuk Choi, Young Kyung Bae
{"title":"Superficial CD34-Positive Fibroblastic Tumor: Two Case Reports.","authors":"Jung Eun Yim,&nbsp;Hyeong Mok Kwon,&nbsp;Hye Ri Kim,&nbsp;Dong Hoon Shin,&nbsp;Jong Soo Choi,&nbsp;Joon Hyuk Choi,&nbsp;Young Kyung Bae","doi":"10.5021/ad.20.328","DOIUrl":"10.5021/ad.20.328","url":null,"abstract":"<p><p>Superficial CD34-positive fibroblastic tumor (SCPFT) is a recently described disease entity characterized by marked nuclear pleomorphism, low mitotic count, and diffuse CD34 positivity. It is a rare, distinctive, low-grade fibroblastic neoplasm. To date, only 44 cases have been reported in the English-language literature. Herein, we report two cases of SCPFT involving a 48-year-old male and a 22-year-old male with superficial tumors on the right and left thighs, respectively. Excision was performed in both cases. Histologically, both tumors showed spindle-to-epithelioid cells arranged in fascicular or sheet-like patterns. Most cells displayed granular or eosinophilic glassy cytoplasm, marked nuclear pleomorphism, and a low mitotic rate. On immunohistochemical staining, tumor cells were diffusely positive for CD34 and negative for S100 protein, smooth muscle actin, and desmin. After wide excision, neither patient experienced recurrence or metastasis after 16 months and 11 months of clinical follow-up, respectively. To the best of our knowledge, these are the first two cases of SCPFT reported in Korea. We believe these case reports would contribute to the clinicopathological understanding of SCPFT and assist clinicians in differentiating this tumor from other superficial soft tissue neoplasms.</p>","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S25-S29"},"PeriodicalIF":0.0,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a8/bf/ad-35-S25.PMC10608372.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49687082","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case of Zosteriform Spiradenoma Following Varicose Veins. 静脉曲张后带状螺旋腺瘤1例。
Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21.006
Su-Hyuk Yim, Seung-Mee Kim, Sanghyun Park, Dongkyun Hong, Kyung Eun Jung, Young Lee, Young-Joon Seo
{"title":"A Case of Zosteriform Spiradenoma Following Varicose Veins.","authors":"Su-Hyuk Yim,&nbsp;Seung-Mee Kim,&nbsp;Sanghyun Park,&nbsp;Dongkyun Hong,&nbsp;Kyung Eun Jung,&nbsp;Young Lee,&nbsp;Young-Joon Seo","doi":"10.5021/ad.21.006","DOIUrl":"10.5021/ad.21.006","url":null,"abstract":"","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S140-S141"},"PeriodicalIF":0.0,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/3f/26/ad-35-S140.PMC10608400.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49686954","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case of Neutrophil-Rich Anaplastic Large-Cell Lymphoma with Relapse. 一例富含中性粒细胞的变性大细胞淋巴瘤复发。
Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21a.028
Jung Eun Seol, Seong Min Hong, Sang Woo Ahn, Jong Uk Kim, Gyeong Je Cho, Woo Jung Jin, So Hee Park, Hyojin Kim
{"title":"A Case of Neutrophil-Rich Anaplastic Large-Cell Lymphoma with Relapse.","authors":"Jung Eun Seol,&nbsp;Seong Min Hong,&nbsp;Sang Woo Ahn,&nbsp;Jong Uk Kim,&nbsp;Gyeong Je Cho,&nbsp;Woo Jung Jin,&nbsp;So Hee Park,&nbsp;Hyojin Kim","doi":"10.5021/ad.21a.028","DOIUrl":"10.5021/ad.21a.028","url":null,"abstract":"<p><p>After anaplastic large-cell lymphoma (ALCL) was first described by Stain in 1985, there have been several histological variants of ALCL reported. There are classified histological subtypes of ALCL, such as lymphohistiocytic, small cell, Hodgkin-like, composite pattern, and other less common variants including neutrophil-rich ALCL. A 63-year-old male patient presented with erythematous exophytic mass on the left lower leg. In the past, his condition had been diagnosed as abdominal primary cutaneous ALCL (pcALCL), which recurred as systemic ALCL (sALCL) in the left bronchus. After treatment, he achieved complete remission. Histopathologic examination showed large-sized pleomorphic, anaplastic mitotic tumor cells, several neutrophils, and a few lymphocytes. Neutrophil-rich ALCL is a rare histological variant of ALCL. It is characterized by the presence of CD30-positive anaplastic tumor cells with numerous neutrophil infiltrations. Neutrophil-rich ALCL responds well to treatment but tends to recur. There were four cases reported to have recurrent neutrophil-rich ALCL. All cases were diagnosed with neutrophil-rich pcALCL prior to recurrence. Three cases had local recurrence, and only one case relapsed as sALCL. Herein, we present the first case of neutrophil-rich ALCL recurring as sALCL twice.</p>","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S76-S78"},"PeriodicalIF":0.0,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/95/d3/ad-35-S76.PMC10608385.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49687012","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case of Atypical Granuloma Annulare Presenting As Palmoplantar Pustules. 一例不典型环状肉芽肿表现为掌跖肿胀。
Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21.029
Joong Ho Kim, Ji An Uh, Jae Ho Lee, Ho Young Kim, Soo Kyung Lee, Myoung Shin Kim, Un Ha Lee
{"title":"A Case of Atypical Granuloma Annulare Presenting As Palmoplantar Pustules.","authors":"Joong Ho Kim,&nbsp;Ji An Uh,&nbsp;Jae Ho Lee,&nbsp;Ho Young Kim,&nbsp;Soo Kyung Lee,&nbsp;Myoung Shin Kim,&nbsp;Un Ha Lee","doi":"10.5021/ad.21.029","DOIUrl":"10.5021/ad.21.029","url":null,"abstract":"Granuloma annulare (GA) is an inflammatory skin disease characterized by ring-shaped, skin-colored to erythematous papules or plaques. GA is clinically classified into localized, generalized, subcutaneous, perforating, and patch types. However, it occasionally shows non-typical patterns such as palmoplantar, blaschkolinear, pustular, and visceral types 1 . Here","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S126-S128"},"PeriodicalIF":0.0,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/da/f1/ad-35-S126.PMC10608401.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49687009","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cutaneous Cytomegalovirus Infection Presenting As Recalcitrant Bullous Pemphigoid Lesion. 皮肤巨细胞病毒感染表现为顽固性大疱性类天疱疮。
Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21.016
Gayun Baek, Taehan Koo, Min-Soo Kim, Mihn-Sook Jue
{"title":"Cutaneous Cytomegalovirus Infection Presenting As Recalcitrant Bullous Pemphigoid Lesion.","authors":"Gayun Baek,&nbsp;Taehan Koo,&nbsp;Min-Soo Kim,&nbsp;Mihn-Sook Jue","doi":"10.5021/ad.21.016","DOIUrl":"10.5021/ad.21.016","url":null,"abstract":"<p><p>Cytomegalovirus (CMV) infection is common among immunocompromised hosts; however, its cutaneous manifestation is considered rare in comparison to internal organ involvement. Clinical manifestations of cutaneous CMV infection generally include perioral or perianal ulcerations. On the other hand, autoimmune bullous dermatosis can have bullae and ulcerations similar to those caused by cutaneous CMV infection. Autoimmune bullous dermatosis requires treatment with immunosuppressive agents for relatively long periods, which may cause reduction of immunocompetence. Because of this iatrogenic immunosuppression, patients with autoimmune bullous dermatosis subsequently acquire increased risk for opportunistic infections. However, cases of bullous pemphigoid (BP) complicated by cutaneous CMV infection are rarely reported. Herein, we report the case of an 88-year-old male who had BP and subsequently recalcitrant perianal skin lesions, which were eventually diagnosed as cutaneous CMV infections.</p>","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S97-S99"},"PeriodicalIF":0.0,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/b8/d8/ad-35-S97.PMC10608396.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49687054","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
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