Annals of dermatology最新文献_第10页

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, Seong Min Hong, Sang Woo Ahn, Jong Uk Kim, Gyeong Je Cho, Woo Jung Jin, So Hee Park, Hyojin Kim","doi":"10.5021/ad.21a.028","DOIUrl":"10.5021/ad.21a.028","url":null,"abstract":"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.","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

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

引用次数: 1

Dermoscopy for the Diagnosis of Creeping Hair Caused by Ingrowing Hair: A Case Report. 皮肤镜检查诊断毛发侵入引起的爬毛：一例报告。

Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21.036

Lijuan Xu, Xinhai Liu, Wei Zhu, Lingling Zheng

{"title":"Dermoscopy for the Diagnosis of Creeping Hair Caused by Ingrowing Hair: A Case Report.","authors":"Lijuan Xu, Xinhai Liu, Wei Zhu, Lingling Zheng","doi":"10.5021/ad.21.036","DOIUrl":"10.5021/ad.21.036","url":null,"abstract":"Creeping hair is a rare condition characterized by creeping eruption with a black line at the advancing end, mimicking cutaneous larva migrans. The condition is also referred to as cutaneous pili migrans, migrating hair, and embedded hair. A total of 52 cases have been reported since 1957 and most cases were published in English. Herein, we report a case in which creeping hair occurred in the iliac region and review the literature from 1957 to February 2021. A 35-year-old Chinese female presented with a black moving linear eruption that had migrated from the lower abdomen to the iliac region without causing any symptoms during a 3-year period. Cutaneous examination showed a 6.5-cm-long black linear lesion beneath the skin that was revealed to be a hair shaft. After removal of the hair, the eruption diminished and no recurrence occurred in 3 months of follow-up. The creeping hair that had migrated with its lower end forward was confirmed by observation under dematoscopy and light microscopy. A review of the literature revealed that creeping hair occurs most frequently in young and middle-aged patients and the reported cases are mainly from Asia. The top locations involve the foot. The causative hair includes head hair, beard, pubic hair, body hair, and one case of dog hair. A close-up examination and dermoscopic inspection are helpful for the diagnosis of creeping hair.","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S112-S116"},"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/6f/0c/ad-35-S112.PMC10608377.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49687055","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

Development of Demodicosis after Omalizumab Injection. 奥马珠单抗注射后Demodicosis的发展。

Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21.027

Sujin Park, Yeongjoo Oh, Howard Chu, Chang Ook Park

引用次数: 0

Dual Biological Therapy for Ulcerative Colitis with Intractable Pyoderma Gangrenosum. 难治性硬皮病并发溃疡性结肠炎的双重生物治疗。

Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21.060

Hae Chan Lee, Yiyoung Kwon, Eun Sil Kim, Soomin Ahn, Yon Ho Choe, Mi Jin Kim

引用次数: 0

Hereditary Leiomyomatosis and Renal Cell Cancer: A Case Report of Pilar Leiomyomatosis with History of Kidney Cancer and Review of the Literature. 遗传性平滑肌瘤病和肾细胞癌症：一例有癌症病史的Pilar平滑肌病病例报告和文献回顾。

Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.20.287

Jee-Woo Kim, Jung-Won Shin, Anna Cho, Chang-Hun Huh

{"title":"Hereditary Leiomyomatosis and Renal Cell Cancer: A Case Report of Pilar Leiomyomatosis with History of Kidney Cancer and Review of the Literature.","authors":"Jee-Woo Kim, Jung-Won Shin, Anna Cho, Chang-Hun Huh","doi":"10.5021/ad.20.287","DOIUrl":"10.5021/ad.20.287","url":null,"abstract":"Pilar leiomyoma or piloleiomyoma is a benign neoplasm of the smooth muscle arising from the arrector pili muscle. It manifests as brown to red firm papulonodules with sites of predilection being the face, trunk, and extensor surfaces of the extremities. Histologically, the lesions exhibit ill-defined dermal tumors with interlacing fascicles of spindle cells. Some genodermatoses are characterized by the development of visceral tumors and cutaneous leiomyomatosis such as Reed's syndrome, and hereditary leiomyomatosis and renal cell cancer (HLRCC). A 55-year-old male presented with reddish-brown papules and nodules on the face and upper back, accompanied by sharp episodic pain on the face. He had undergone nephrectomy for renal cancer 9 years ago, and his younger brother had similar cutaneous manifestation. Histopathologic findings were consistent with pilar leiomyoma, showing bundles of smooth muscle tumors in the dermis. Based on the clinical information including clinical features, past medical history, and family history, HLRCC was highly suspected. To confirm the diagnosis, whole exome sequencing was performed using peripheral blood, which revealed a novel point mutation (c.739G>A, p.Glu247Lys) in the fumarate hydratase (FH) gene. We describe a confirmed case of HLRCC, which is a genetic disorder with a potential to cause visceral cancers, which dermatologists might overlook as a benign condition.","PeriodicalId":94298,"journal":{"name":"Annals of dermatology","volume":"35 Suppl 1","pages":"S14-S18"},"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/05/95/ad-35-S14.PMC10608374.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49687063","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

Primary Cutaneous Apocrine Carcinoma and Syringocystadenoma Papilliferum Arising in Nevus Sebaceus: A Case Report and Review of the Literature. Sebaseus原发性皮肤顶泌癌和乳头状囊腺瘤：一例病例报告和文献复习。

Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21.039

Jee Woo Kim, Jung Won Shin, Chang-Hun Huh

引用次数: 0

The Consideration for an Unlikely Culprit Drug (Betahistine) Inducing Toxic Epidermal Necrolysis: A Case Report. 对一种不太可能诱导毒性表皮坏死松解的朊病毒药物（倍他司汀）的考虑：一例报告。

Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.20.247

Tetsuharu Ikegami, Shujiro Hayashi, Maki Okamoto, Junko Kanai, Yuki Kaneko, Yuki Saito, Tomoko Kaminaga, Youichiro Hamasaki, Ken Igawa

引用次数: 1

Unilateral Psoriasis on the Left Leg and Poliomyelitis of the Right Leg: A Case Report and Review of the Etiology. 单侧左腿银屑病和右腿脊髓灰质炎：一例病例报告和病因回顾。

Annals of dermatology Pub Date : 2023-05-01 DOI: 10.5021/ad.21.174

Jongwook Kim, Kyung-Nam Bae, Jin-Hwa Son, Kihyuk Shin, Hoon-Soo Kim, Hyun-Chang Ko, Moon-Bum Kim, Byungsoo Kim

引用次数: 0