eccrine duct

  • 文章类型: Case Reports
    汗管瘤是起源于内分泌导管的良性肿瘤。下眼睑是最常见的起源部位。迄今为止,文献中报道的病例很少。组织病理学表明,纤维囊中的正常压缩内分泌导管以及排列在小管和实心岛中的肿瘤细胞。本报告描述了一例女性患者下眼睑的汗管瘤。
    Syringomas are benign tumours originating from the eccrine ducts. Lower eyelid is the commonest site of origin. Very few cases have been reported in literature till date. Histopathology demonstrates normal compressed eccrine ducts in the fibrous capsule along with tumour cells arranged in tubules and solid islands. This report describes a case of syringoma on the lower eyelid in a female patient.
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  • 文章类型: Case Reports
    猴痘历史上被认为是一种人畜共患疾病,仅限于有动物水库的地区,人类传播的可能性有限。然而,最近非流行地区的发病率增加,连同人类传播的演示,引起了人们对这种疾病的更多关注。我们介绍了一个27岁的男性皮肤病变和肛周溃疡,临床上提示病毒性疾病。用PCR分析证明猴痘。讨论了猴痘的组织学特征和鉴别诊断,并描述了内分泌腺上皮的特征性组织病理学模式,如果在溃疡病变中发现,应该引起猴痘的怀疑.
    Monkeypox was historically considered a zoonotic disease restricted to areas with an animal reservoir and with limited possibilities of human transmission. However, the recent increase in incidence in non-endemic areas, together with the demonstration of human transmission, has led to more attention being paid to this disease. We present the case of a 27-year-old man with cutaneous lesions and perianal ulcers, clinically suggestive of a viral disease. Monkeypox was demonstrated with PCR analysis. The histological features and differential diagnoses of monkeypox are discussed and the characteristic histopathological pattern of eccrine gland epithelium is described which, if found in an ulcerated lesion, should raise suspicion of monkeypox.
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  • 文章类型: Case Reports
    皮肤通常受移植物抗宿主病(GVHD)的影响,骨髓移植(BMT)的并发症。三分之一的造血细胞移植受者发生急性喷发,通常被描述为卵泡中心,斑丘疹,或者男性,与更常见的硬化慢性表现相反,polikilodermic,或苔藓类皮肤。随着非清髓性(降低强度)移植治疗的广泛使用,可能会出现各种非典型的表现,代表诊断挑战。在这里,我们报告了一例罕见的慢性GVHD病例,表现为两种不同的临床和组织病理学特征,缺乏经典表现。她的BMT后五个月,病人的脖子上出现了丘疹鳞状皮疹,树干,和显示慢性GVHD的银屑病样组织病理学模式的手臂。她还在远端四肢上表现出多个小的肉色丘疹,显示出孤立的促注射器型GVHD,表现为涉及浅表内分泌导管的界面性皮炎,作为GVHD的唯一诊断性组织病理学特征。这份报告,通过文献回顾,突出了罕见的银屑病样GVHD和孤立的促注射器性慢性GVHD的新颖描述。
    Skin is commonly affected by graft versus host disease (GVHD), a complication of bone marrow transplantation (BMT). One-third of hematopoietic cell transplantation recipients develop acute eruption classically described as folliculocentric, maculopapular, or morbilliform, in contrast to the more common chronic presentations of sclerotic, poikilodermic, or lichenoid dermatitides. With the wider use of non-myeloablative (reduced-intensity) transplant therapy, various atypical presentations can occur, representing a diagnostic challenge. Herein, we report an unusual case of chronic GVHD manifested by two distinct clinical and histopathological features lacking the classical presentation. Five months after her BMT, the patient presented with a papulosquamous eruption on her neck, trunk, and arms showing a psoriasiform histopathological pattern of chronic GVHD. She also demonstrated multiple small flesh-colored papules on her distal extremities showing a solitary syringotropic pattern of GVHD, demonstrated by interface dermatitis involving the superficial eccrine duct, as the only diagnostic histopathological feature of GVHD. This report, with review of literature, highlights the uncommon psoriasiform GVHD and the novel description of isolated syringotropic chronic GVHD.
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  • 文章类型: Journal Article
    背景:汗管瘤是一种良性附件肿瘤,被认为是安全的,恶性可能性非常低。然而,多个微小病变通常会影响面部和暴露区域,这可能会引起患者的美容问题。经过临床诊断,有两种诊断方法:细针穿刺细胞学(FNAC)和组织病理学。FNAC通常用于汗管瘤的初步评估,而组织病理学被用作诊断汗管瘤的确证试验。在开发和资源有限的环境中,FNAC和组织病理学的结合将造成财务和物流负担。目的本研究旨在观察三级医院临床诊断为汗管瘤的病例的细胞学和组织病理学特征,以建议使用FNAC或组织病理学诊断汗管瘤。材料与方法本横断面观察性研究于2021年11月至2022年4月在印度东部一家三级保健医院的皮肤科和病理科进行。在获得自愿参与的知情同意后,招募任何临床上临时诊断的汗管瘤病例进行研究。采取无菌预防措施,在皮肤科进行组织抽吸和穿刺活检,并将样本送至病理科.细胞学和组织学检查由一名专家病理学家进行。结果共50例(女性36例,研究包括14名男性),中位年龄为23岁(范围10-40岁)。共有43例出现丘疹性病变,7例出现结节。在大多数情况下(40%),病变位于眼睑,其次是手臂的26%。在FNAC,发现附件良性病变22例,16个暗示了汗管瘤,八人被诊断为黄色瘤,两个被诊断为疣,有两个案例没有足够的意见。组织学上,42例确诊为汗管瘤,六个被诊断为黄色瘤,两例被诊断为疣。FNAC诊断与组织病理学之间存在显着差异(McNemarχ2=24.038,p值=0.0001)。结论FNAC与汗管瘤的组织病理学诊断可能无法证实。良性附件病变难以通过FNAC进行分类。临床诊断的汗管瘤病例的组织病理学检查有助于明确诊断。因此,为了节省患者的时间和不适,可以避免FNAC,并且临床诊断病例可以通过组织病理学检查来诊断。
    Background Syringoma is a benign adnexal neoplasm and is considered safe with very low malignant potential. However, multiple tiny lesions typically affect the face and exposed area, which may cause a cosmetic concern for the patient. After a clinical diagnosis, there are two methods to diagnose syringoma: fine needle aspiration cytology (FNAC) and histopathology. FNAC is generally used for the initial evaluation of syringoma, while histopathology is used as a confirmatory test to diagnose syringoma. In developing and resource-limited settings, the combination of FNAC and histopathology would cause a financial and logistics burden. Objective This study aimed to observe the cytological and histopathological features of cases clinically diagnosed as syringomas in a tertiary care hospital to suggest the use of either FNAC or histopathology for diagnosing syringoma. Materials and Methods This cross-sectional observational study was conducted in the Department of Dermatology and Department of Pathology of a tertiary care hospital in eastern India from November 2021 to April 2022. Any clinically provisionally diagnosed case of syringoma was recruited for the study after obtaining informed consent for voluntary participation. With aseptic precautions, the tissue aspirates and punch biopsy were obtained in the Department of Dermatology and the samples were sent to the Department of Pathology. Cytological and histological examination was conducted by a single expert pathologist. Result A total of 50 cases (36 female, 14 male) with a median age of 23 years (range 10-40 years) were included in the study. A total of 43 cases were presented with papular lesions and seven with nodules. In the majority of the cases (40%), the lesion was in the eyelid followed by 26% in the arm. In FNAC, 22 cases were found to be benign adnexal lesions, 16 were suggestive of syringoma, eight were diagnosed as xanthoma, two were diagnosed as warts, and two cases were inadequate for opinion. Histologically, 42 cases were confirmed as syringoma, six were diagnosed as xanthoma, and two cases were diagnosed as warts. There was a significant difference between diagnosis by FNAC and histopathology (McNemar χ2 = 24.038, p-value = 0.0001). Conclusion We found that FNAC and histopathological diagnosis of syringoma may not be corroborative. Benign adnexal lesions are difficult to categorize by FNAC. Histopathological examination of clinically diagnosed cases of syringoma is of help for definitive diagnosis. Hence, FNAC may be avoided for saving time and discomfort for the patients and clinically diagnosed cases may be diagnosed by histopathological examination.
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  • 文章类型: Case Reports
    汗管瘤是起源于内分泌汗腺导管的表皮内部分的良性肿瘤。一名6岁的非洲裔美国女性颈部出现多个2-3毫米色素沉着丘疹,上胸部,和两侧的腋窝。病变没有触痛,非瘙痒,轻轻刮擦时没有流血。偶然在患者的中背发现了一个咖啡斑。组织病理学,在苏木精和曙红染色中发现了多个小导管,这些导管显示出a形/佩斯利领带图案并伴有纤维化基质。还鉴定了上皮,其显示出具有基底细胞样外观的细胞巢和充满嗜酸性物质的腺体。这些组织病理学发现与发疹性汗管瘤的诊断一致。病人接受了保守治疗,病变在没有干预的情况下消退。在大多数要求治疗的患者中,使用异维A酸;然而,这对许多患者来说可能是不必要的措施。总的来说,由于患者的年龄较小,该病例意义重大,种族,以及在没有治疗的情况下的临床改善。
    Syringomas are benign tumors originating from the intraepidermal portion of eccrine sweat ducts. A six-year-old African American female presented with multiple 2-3 mm hyperpigmented papules over the neck, upper chest, and axillae bilaterally. The lesions were non-tender, non-pruritic, and did not bleed when lightly scraped. A café-au-lait macule was incidentally found in the mid-back of the patient. Histopathologically, multiple small ducts displaying a tadpole-shaped/paisley-tie pattern with fibrotic stroma were identified on hematoxylin and eosin staining. Epithelium showing nests of cells with basaloid appearance and dilated glands filled with eosinophilic material were also identified. These histopathologic findings were consistent with a diagnosis of eruptive syringoma. The patient was treated conservatively, and the lesions subsided without intervention. In most patients requesting treatment, isotretinoin is used; however, this may be an unnecessary measure in many patients. Overall, this case was significant due to the patient\'s young age, ethnicity, and clinical improvement in the absence of treatment.
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  • 文章类型: Comparative Study
    BACKGROUND: Eccrine duct dilatation (EDD) has been noted to occur significantly more often in primary lymphocytic scarring alopecias compared with non-scarring alopecias, thus serving as a possible histopathologic marker for primary scarring alopecias with a lymphocytic infiltrate. This study aims to determine the presence and role of EDD in primary neutrophilic scarring alopecias.
    METHODS: We performed a retrospective review comparing primary scarring alopecia (neutrophilic, n = 90; lymphocytic, n = 100) and non-scarring alopecia (n = 123) for presence of EDD, seen in Boston University School of Medicine between 2013 and 2017.
    RESULTS: EDD was more commonly seen in primary neutrophilic scarring (62.2%, 56/90) and primary lymphocytic scarring alopecias (54.0%, 54/100) than in non-scarring alopecias (25.2%, 31/123) (P < 0.001). Albeit uncommon, non-scarring alopecias exhibited the biggest ratio of dilated eccrine duct lumen to background duct lumen (14.33), followed by lymphocytic (10.99) and neutrophilic scarring alopecias (6.66).
    CONCLUSIONS: EDD is seen more frequently in primary scarring alopecias compared with non-scarring alopecias and usually found in sections containing inflammation and dermal fibrosis, serving as a possible histopathologic clue for a scarring process. Non-scarring alopecias have significantly fewer but considerably larger EDD which, may imply a different pathologic cause.
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