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Hidradenocarcinoma of the Chest With Axillary Lymph Node Metastasis: Report of 2 Cases and Systematic Literature Review of a Breast Cancer Mimicker. 胸部汗腺癌伴腋窝淋巴结转移:2例报告及1例乳腺癌模拟者的系统文献复习。
IF 1.1 4区 医学 Q4 DERMATOLOGY Pub Date : 2024-12-10 DOI: 10.1097/DAD.0000000000002874
Francesco Fortarezza, Giuseppe Maggioni, Anna Colagrande, Gerardo Cazzato, Angelo Paolo Dei Tos

Abstract: Hidradenocarcinoma (HAC) is a rare malignant neoplasm originating from eccrine sweat glands, often presenting diagnostic challenges because of its resemblance to other malignancies, particularly breast cancer when occurring in the chest region. This report describes 2 cases of HAC with axillary lymph node metastasis, both initially misinterpreted clinically. The first case involved a 63-year-old woman with a sternal mass, near the right breast, initially suspected to be a sebaceous cyst. Histologic examination revealed a solid-cystic epithelial tumor with features suggestive of HAC, confirmed by immunohistochemical analysis. The second case concerned an 81-year-old woman with a subcutaneous growth in the sternal area, also diagnosed as HAC after histopathologic and immunohistochemical assessment. Both cases demonstrated strong estrogen receptor positivity, leading to the recommendation of hormonal therapy. A systematic review of the literature identified 21 similar cases of HAC in the chest wall, highlighting the diagnostic complexities and the potential for these tumors to mimic breast carcinoma. This review underscores the need for careful histologic and immunohistochemical evaluation to differentiate HAC from other malignancies, particularly in the breast region. Given the rare and the potential aggressive nature of HAC, early and accurate diagnosis is crucial for guiding appropriate therapeutic strategies and improving patient outcomes.

摘要:汗腺癌(Hidradenocarcinoma, HAC)是一种罕见的起源于内分泌汗腺的恶性肿瘤,由于其与其他恶性肿瘤,特别是发生在胸部区域的乳腺癌相似,经常给诊断带来挑战。本文报告2例HAC伴腋窝淋巴结转移的病例,均为临床误诊。第一例患者为63岁女性,右乳附近胸骨肿块,最初怀疑为皮脂腺囊肿。组织学检查显示一个实体囊性上皮肿瘤,具有提示HAC的特征,免疫组织化学分析证实。第二个病例涉及一名81岁女性,胸骨区皮下生长,经组织病理学和免疫组织化学评估后也诊断为HAC。这两例均表现出强烈的雌激素受体阳性,因此推荐激素治疗。对文献的系统回顾发现了21例类似的胸壁HAC病例,强调了诊断的复杂性和这些肿瘤模仿乳腺癌的可能性。这篇综述强调需要仔细的组织学和免疫组织化学评估来区分HAC与其他恶性肿瘤,特别是在乳房区域。鉴于HAC的罕见性和潜在的侵袭性,早期和准确的诊断对于指导适当的治疗策略和改善患者预后至关重要。
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引用次数: 0
PRAME as a Diagnostic Marker in Desmoplastic Melanocytic Lesions: Insights and Challenges. PRAME作为促结缔组织增生黑色素细胞病变的诊断标志物:见解和挑战。
IF 1.1 4区 医学 Q4 DERMATOLOGY Pub Date : 2024-12-10 DOI: 10.1097/DAD.0000000000002904
Şule Öztürk Sarı, Ali Kubilay Kolik, Begüm Yeni Erdem, Nesimi Büyükbabani
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引用次数: 0
The Prognostic Significance of Tumor Budding and Tumor-Infiltrating Lymphocytes in Patients Diagnosed With Malignant Melanoma. 恶性黑色素瘤患者肿瘤萌芽和肿瘤浸润淋巴细胞的预后意义。
IF 1.1 4区 医学 Q4 DERMATOLOGY Pub Date : 2024-12-10 DOI: 10.1097/DAD.0000000000002902
Ayşen Yavuz, Kübra Şimşek, Cumhur İbrahim Başsorgun, Gülsüm Özlem Elpek, Betül Ünal

Abstract: The tumor microenvironment plays a critical role in malignant melanoma, influencing progression and patient outcomes, particularly through tumor budding (TB) and tumor-infiltrating lymphocytes (TILs). Despite the importance of TB, its detailed impact still needs to be explored, especially its interaction with TILs. This study evaluates the prognostic significance of TB and TILs in malignant melanoma, assessing their potential as indicators for disease progression and survival. Conducted at Akdeniz University, the research included 92 patients diagnosed between 2014 and 2021. TB was evaluated according to the International Tumor Budding Consensus Conference guidelines, and TILs were assessed by the International Immuno-Oncology Biomarker Working Group standards. The analysis revealed significant correlations between TB and the level of anatomic invasion, Breslow thickness, satellite nodules, lymph node metastasis, distant metastasis, and stage (P < 0.05). A notable inverse relationship between TB and intratumoral TILs suggested their different roles in tumor progression. Tumor subtype, level of anatomic invasion, satellite nodules, lymphovascular invasion, lymph node metastasis, distant metastasis, stage, TILs, and TB were significant risk factors associated with poor prognosis (P < 0.005). Multivariate Cox regression identified histologic subtype and TB >10 as independent prognostic factors, underscoring the need for further research to integrate TB and TILs into clinical practice for better patient management and treatment planning.

摘要:肿瘤微环境在恶性黑色素瘤中起着关键作用,特别是通过肿瘤出芽(TB)和肿瘤浸润淋巴细胞(TILs)影响其进展和患者预后。尽管结核病很重要,但其具体影响仍需探索,特别是与TILs的相互作用。本研究评估了TB和TILs在恶性黑色素瘤中的预后意义,评估了它们作为疾病进展和生存指标的潜力。在Akdeniz大学进行的这项研究包括了2014年至2021年间诊断出的92名患者。结核病根据国际肿瘤萌芽共识会议指南进行评估,TILs根据国际免疫肿瘤生物标志物工作组标准进行评估。分析发现结核与解剖浸润程度、Breslow厚度、卫星结节、淋巴结转移、远处转移和分期有显著相关性(P < 0.05)。结核与肿瘤内TILs呈显著的负相关,表明它们在肿瘤进展中的作用不同。肿瘤亚型、解剖浸润程度、卫星结节、淋巴血管浸润、淋巴结转移、远处转移、分期、TILs、TB是预后不良的重要危险因素(P < 0.005)。多因素Cox回归发现,组织学亚型和TB bbb10是独立的预后因素,强调需要进一步研究将结核病和TILs纳入临床实践,以更好地管理患者和制定治疗计划。
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引用次数: 0
Diagnostic Accuracy of ChatGPT for Textbook Descriptions of Epidermal Tumors: Correspondence. 表皮肿瘤教科书描述的 ChatGPT 诊断准确性:通信。
IF 1.1 4区 医学 Q4 DERMATOLOGY Pub Date : 2024-12-01 Epub Date: 2024-08-14 DOI: 10.1097/DAD.0000000000002829
Hinpetch Daungsupawongm, Viroj Wiwanitkit
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引用次数: 0
Adding "Unlikely" as a Clinical Qualifier Is Unlikely to Be of Help: A Retrospective, Single-Center, Cross-Sectional Cohort Study. 添加 "不太可能 "作为临床修饰词不太可能有帮助:一项回顾性、单中心、横断面队列研究。
IF 1.1 4区 医学 Q4 DERMATOLOGY Pub Date : 2024-12-01 Epub Date: 2024-08-14 DOI: 10.1097/DAD.0000000000002814
Jinpyo Hong, Joshua Shoemaker, Jennifer Scott, Klaus Helm

Abstract: Clinical correlation is essential to accurate and efficient diagnosis and differential diagnosis in dermatopathology. Poor-quality clinical information can lead to failures and delays in patient care. Some clinicians use the term "unlikely" when submitting a specimen. How frequently the "unlikely" clinical diagnosis correlates with the final pathologic diagnosis is unknown. We studied 203 dermatopathology reports from December 8, 2020, to July 1, 2021, that included the qualifier "unlikely" on the requisition sheet. Samples were stratified into either an inflammatory or neoplastic cohort based on final histopathologic diagnosis, with the neoplastic cohort being further stratified into pigmented and nonpigmented cohorts. Statistical analyses were conducted. The "unlikely" diagnosis in the clinical differential diagnosis and the final histologic diagnosis were the same in 7.9% of the 203 samples studied. This occurred in 8.5% of the inflammatory cohort and 7.6% of the neoplastic cohort. We concluded that the use of the qualifier "unlikely" is not helpful. We acknowledge the limitations of our study because of a small sample.

摘要:在皮肤病理学中,临床相关性对于准确有效的诊断和鉴别诊断至关重要。低质量的临床信息会导致患者治疗的失败和延误。一些临床医生在提交标本时使用 "不太可能 "一词。但 "不太可能 "的临床诊断与最终病理诊断的相关性有多大还不得而知。我们对 2020 年 12 月 8 日至 2021 年 7 月 1 日期间的 203 份皮肤病理报告进行了研究,这些报告在申购单上包含 "不太可能 "的限定词。根据最终的组织病理学诊断,我们将样本分为炎症性样本和肿瘤性样本,其中肿瘤性样本又分为色素性样本和非色素性样本。进行了统计分析。在所研究的 203 个样本中,有 7.9% 的样本临床鉴别诊断中的 "不太可能 "诊断与最终组织学诊断相同。这种情况在炎症性样本中占 8.5%,在肿瘤性样本中占 7.6%。我们的结论是,使用 "不太可能 "这一修饰词没有帮助。我们承认,由于样本较少,我们的研究存在局限性。
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引用次数: 0
Pseudolipoblastic Perineuroma: A Rare Histologi̇c Subtype. 假脂母细胞性会阴瘤:一种罕见的组织学亚型。
IF 1.1 4区 医学 Q4 DERMATOLOGY Pub Date : 2024-12-01 Epub Date: 2024-10-15 DOI: 10.1097/DAD.0000000000002857
Ozlem Erdem, Barbara Corti, Francesco Paolo Salamone, Bianca Maria Piraccini, Cosimo Misciali

Abstract: Pseudolipoblastic perineurioma is a very uncommon variant of extraneural perineurioma, with only a limited number of cases documented in the medical literature. The most remarkable histopathologic characteristic is the existence of vacuolated cells that closely resemble lipoblasts; besides the presence of small, spindle shaped, or epithelioid perineurial cells. In this study, we present another case of pseudolipoblastic perineurioma, predominantly characterized by the presence of vacuolated "pseudolipoblastic" cells. The immunohistochemical expression of EMA, Glut-1, claudin-1, collagen type IV, and laminin as well as S-100 negativity is essential for the diagnosis to support the perineurial origin. Simple excision is the best treatment option for these benign tumors that do not recur or metastasize. It is crucial to recognize this rare entity to differentiate it from many other tumors characterized by prominent intracytoplasmic vacuoles.

摘要:假性脂母细胞性会阴瘤是会阴外肿瘤的一种非常罕见的变异型,医学文献中仅记载了有限的几例。其最显著的组织病理学特征是存在空泡细胞,与脂肪母细胞非常相似;此外,还存在小的、纺锤形或上皮样的会阴部细胞。在本研究中,我们发现了另一例假脂母细胞性会厌瘤,其主要特征是存在空泡化的 "假脂母细胞"。EMA、Glut-1、claudin-1、IV 型胶原和层粘连蛋白的免疫组化表达以及 S-100 阴性是诊断的关键,以支持会厌起源。对于这些不会复发或转移的良性肿瘤,简单切除是最佳治疗方案。识别这种罕见的肿瘤,将其与许多其他以突出胞浆内空泡为特征的肿瘤区分开来至关重要。
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引用次数: 0
Clinicopathologic Correlation and Routine Immunostains Help Distinguish Congenital Disseminated Pyogenic Granuloma From Other Cutaneous Disseminated Vascular Proliferations of Infancy: Case Report and Literature Review. 临床病理相关性和常规免疫印迹有助于区分先天性播散性化脓性肉芽肿和其他婴儿期皮肤播散性血管增生:病例报告和文献综述。
IF 1.1 4区 医学 Q4 DERMATOLOGY Pub Date : 2024-12-01 Epub Date: 2024-08-14 DOI: 10.1097/DAD.0000000000002830
Kristan Schiele, Veronica Voronina, Arthur Marka, Julianne Mann, Robert E LeBlanc

Abstract: The presence of multiple cutaneous vascular lesions in infancy can signal the possibility of visceral involvement. Dermatopathologists must appreciate how the differential diagnosis includes entities that have distinct therapeutic and prognostic implications. Fortunately, these rare entities can be distinguished histopathologically with the help of clinicopathologic correlation and immunohistochemistry. In this article, we discuss congenital disseminated pyogenic granuloma, multifocal infantile hemangioma, and multifocal lymphangioendotheliomatosis with thrombocytopenia. Subtle morphologic and immunophenotypic features permit their distinction, which in turn is important for identifying extracutaneous manifestations and effective treatments. We present a case of a 3-week-old infant with congenital disseminated pyogenic granuloma involving the skin and the liver whose lesions regressed without therapeutic intervention over 6 months of close follow-up. We review the literature on these rare, overlapping entities and present an approach to resolving the differential diagnosis.

摘要:婴儿期出现多发性皮肤血管病变可能预示着内脏受累。皮肤病理学家必须了解鉴别诊断如何包括具有不同治疗和预后影响的实体。幸运的是,在临床病理相关性和免疫组化的帮助下,这些罕见的实体可以通过组织病理学加以区分。本文将讨论先天性播散性化脓性肉芽肿、多灶性婴儿血管瘤和伴血小板减少的多灶性淋巴管内皮细胞瘤病。微妙的形态学和免疫表型特征可以将它们区分开来,而这对于确定皮肤外表现和有效治疗也很重要。我们介绍了一例 3 周大婴儿先天性播散性化脓性肉芽肿病例,该病累及皮肤和肝脏,经过 6 个月的密切随访,病变在没有治疗干预的情况下消退。我们回顾了有关这些罕见、重叠实体的文献,并介绍了一种解决鉴别诊断的方法。
{"title":"Clinicopathologic Correlation and Routine Immunostains Help Distinguish Congenital Disseminated Pyogenic Granuloma From Other Cutaneous Disseminated Vascular Proliferations of Infancy: Case Report and Literature Review.","authors":"Kristan Schiele, Veronica Voronina, Arthur Marka, Julianne Mann, Robert E LeBlanc","doi":"10.1097/DAD.0000000000002830","DOIUrl":"10.1097/DAD.0000000000002830","url":null,"abstract":"<p><strong>Abstract: </strong>The presence of multiple cutaneous vascular lesions in infancy can signal the possibility of visceral involvement. Dermatopathologists must appreciate how the differential diagnosis includes entities that have distinct therapeutic and prognostic implications. Fortunately, these rare entities can be distinguished histopathologically with the help of clinicopathologic correlation and immunohistochemistry. In this article, we discuss congenital disseminated pyogenic granuloma, multifocal infantile hemangioma, and multifocal lymphangioendotheliomatosis with thrombocytopenia. Subtle morphologic and immunophenotypic features permit their distinction, which in turn is important for identifying extracutaneous manifestations and effective treatments. We present a case of a 3-week-old infant with congenital disseminated pyogenic granuloma involving the skin and the liver whose lesions regressed without therapeutic intervention over 6 months of close follow-up. We review the literature on these rare, overlapping entities and present an approach to resolving the differential diagnosis.</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":" ","pages":"860-863"},"PeriodicalIF":1.1,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141983803","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}
引用次数: 0
Vulvar Skin Metastasis From Cervical Adenocarcinoma. 宫颈腺癌的外阴皮肤转移。
IF 1.1 4区 医学 Q4 DERMATOLOGY Pub Date : 2024-12-01 Epub Date: 2024-10-15 DOI: 10.1097/DAD.0000000000002846
Zhongyun Deng, Wenjie Li, Xiaomin Tang, Bei Zhao, Juan Li, Zhen Rang, Ge Yang, Wei Liu, Fan Cui

Abstract: Cervical cancer stands as one of the most common gynecologic malignancies in developing countries; however, cutaneous metastasis from cervical cancer is a rare occurrence. In this study, we present a case involving a 44-year-old woman diagnosed with International Federation of Gynecology and Obstetrics stage IIA gastric-type endocervical adenocarcinoma. Two years later, after undergoing radical hysterectomy and chemoradiation therapy, she exhibited cutaneous metastasis in the vulvar region.

摘要:宫颈癌是发展中国家最常见的妇科恶性肿瘤之一,但宫颈癌的皮肤转移却很少发生。在本研究中,我们介绍了一例确诊为国际妇产科联盟 IIA 期胃型宫颈内膜腺癌的 44 岁女性病例。两年后,在接受根治性子宫切除术和化疗放疗后,她的外阴部位出现皮肤转移。
{"title":"Vulvar Skin Metastasis From Cervical Adenocarcinoma.","authors":"Zhongyun Deng, Wenjie Li, Xiaomin Tang, Bei Zhao, Juan Li, Zhen Rang, Ge Yang, Wei Liu, Fan Cui","doi":"10.1097/DAD.0000000000002846","DOIUrl":"10.1097/DAD.0000000000002846","url":null,"abstract":"<p><strong>Abstract: </strong>Cervical cancer stands as one of the most common gynecologic malignancies in developing countries; however, cutaneous metastasis from cervical cancer is a rare occurrence. In this study, we present a case involving a 44-year-old woman diagnosed with International Federation of Gynecology and Obstetrics stage IIA gastric-type endocervical adenocarcinoma. Two years later, after undergoing radical hysterectomy and chemoradiation therapy, she exhibited cutaneous metastasis in the vulvar region.</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":"46 12","pages":"852-854"},"PeriodicalIF":1.1,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142683431","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}
引用次数: 0
Appropriate Statistical Methods to Assess Cross-study Diagnostic 23-Gene Expression Profile Test Performance for Cutaneous Melanocytic Neoplasms. 评估皮肤黑色素细胞肿瘤 23 基因表达谱交叉研究诊断测试性能的适当统计方法。
IF 1.1 4区 医学 Q4 DERMATOLOGY Pub Date : 2024-12-01 Epub Date: 2024-08-14 DOI: 10.1097/DAD.0000000000002808
Matthew S Goldberg, Clay J Cockerell, Jason H Rogers, Jennifer J Siegel, Brooke H Russell, Gregory A Hosler, Etan Marks

Abstract: Comparing studies of molecular ancillary diagnostic tests for difficult-to-diagnose cutaneous melanocytic neoplasms presents a methodological challenge, given the disparate ways accuracy metrics are calculated. A recent report by Boothby-Shoemaker et al investigating the real-world accuracy of the 23-gene expression profile (23-GEP) test highlights this methodological difficulty, reporting lower accuracy than previously observed. However, their calculation method-with indeterminate test results defined as either false positive or false negative-was different than those used in previous studies. We corrected for these differences and recalculated their reported accuracy metrics in the same manner as the previous studies to enable appropriate comparison with previously published reports. This corrected analysis showed a sensitivity of 92.1% (95% confidence interval [CI], 82.1%-100%) and specificity of 94.4% (91.6%-96.9%). We then compared these results directly to previous studies with >25 benign and >25 malignant cases with outcomes and/or concordant histopathological diagnosis by ≥3 dermatopathologists. All studies assessed had enrollment imbalances of benign versus malignant patients (0.8-7.0 ratio), so balanced cohorts were resampled according to the lowest common denominator to calculate point estimates and CIs for accuracy metrics. Overall, we found no statistically significant differences in the ranges of 23-GEP sensitivity, 90.4%-96.3% (95% CI, 80.8%-100%), specificity, 87.3%-96.2% (78.2%-100%), positive predictive value, 88.5%-96.1% (81.5%-100%), or negative predictive value, 91.1%-96.3% (83.6%-100%) between previous studies and the cohort from Boothby-Shoemaker et al with this unified methodological approach. Rigorous standardization of calculation methods is necessary when the goal is direct cross-study comparability.

摘要:对难以诊断的皮肤黑色素细胞肿瘤的分子辅助诊断测试研究进行比较是一项方法学挑战,因为准确性指标的计算方法各不相同。Boothby-Shoemaker 等人最近对 23 基因表达谱(23-GEP)检验的实际准确性进行了调查,报告的准确性低于之前观察到的准确性,这凸显了方法学上的困难。然而,他们的计算方法--将不确定的检测结果定义为假阳性或假阴性--与之前研究中使用的方法不同。我们对这些差异进行了校正,并以与之前研究相同的方式重新计算了他们报告的准确度指标,以便与之前发表的报告进行适当比较。校正后的分析结果显示,灵敏度为 92.1%(95% 置信区间 [CI],82.1%-100%),特异度为 94.4%(91.6%-96.9%)。然后,我们将这些结果直接与之前由≥3 位皮肤病理学家对结果和/或组织病理诊断一致的>25 个良性病例和>25 个恶性病例进行的研究进行了比较。所有被评估的研究都存在良性与恶性患者入组不平衡的问题(0.8-7.0 的比例),因此根据最小公分母对平衡队列进行了重新取样,以计算准确性指标的点估计和 CI。总体而言,我们发现在 23-GEP 灵敏度(90.4%-96.3%,95% CI,80.8%-100%)、特异性(87.3%-96.2%,78.2%-100%)、阳性预测值(88.5%-96.1%,81.5%-100%)或阴性预测值(91.1%-96.3%,83.6%-100%)的范围内,以前的研究与 Boothby-Shoemaker 等人的队列采用这种统一的方法学方法没有明显的统计学差异。如果要实现直接的跨研究可比性,就必须对计算方法进行严格的标准化。
{"title":"Appropriate Statistical Methods to Assess Cross-study Diagnostic 23-Gene Expression Profile Test Performance for Cutaneous Melanocytic Neoplasms.","authors":"Matthew S Goldberg, Clay J Cockerell, Jason H Rogers, Jennifer J Siegel, Brooke H Russell, Gregory A Hosler, Etan Marks","doi":"10.1097/DAD.0000000000002808","DOIUrl":"10.1097/DAD.0000000000002808","url":null,"abstract":"<p><strong>Abstract: </strong>Comparing studies of molecular ancillary diagnostic tests for difficult-to-diagnose cutaneous melanocytic neoplasms presents a methodological challenge, given the disparate ways accuracy metrics are calculated. A recent report by Boothby-Shoemaker et al investigating the real-world accuracy of the 23-gene expression profile (23-GEP) test highlights this methodological difficulty, reporting lower accuracy than previously observed. However, their calculation method-with indeterminate test results defined as either false positive or false negative-was different than those used in previous studies. We corrected for these differences and recalculated their reported accuracy metrics in the same manner as the previous studies to enable appropriate comparison with previously published reports. This corrected analysis showed a sensitivity of 92.1% (95% confidence interval [CI], 82.1%-100%) and specificity of 94.4% (91.6%-96.9%). We then compared these results directly to previous studies with >25 benign and >25 malignant cases with outcomes and/or concordant histopathological diagnosis by ≥3 dermatopathologists. All studies assessed had enrollment imbalances of benign versus malignant patients (0.8-7.0 ratio), so balanced cohorts were resampled according to the lowest common denominator to calculate point estimates and CIs for accuracy metrics. Overall, we found no statistically significant differences in the ranges of 23-GEP sensitivity, 90.4%-96.3% (95% CI, 80.8%-100%), specificity, 87.3%-96.2% (78.2%-100%), positive predictive value, 88.5%-96.1% (81.5%-100%), or negative predictive value, 91.1%-96.3% (83.6%-100%) between previous studies and the cohort from Boothby-Shoemaker et al with this unified methodological approach. Rigorous standardization of calculation methods is necessary when the goal is direct cross-study comparability.</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":" ","pages":"833-838"},"PeriodicalIF":1.1,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11573081/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141983802","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}
引用次数: 0
Oral Myeloid Sarcoma as a Marker of Relapse in Acute Myeloid Leukemia. 作为急性髓性白血病复发标志的口腔髓样肉瘤
IF 1.1 4区 医学 Q4 DERMATOLOGY Pub Date : 2024-12-01 Epub Date: 2024-09-17 DOI: 10.1097/DAD.0000000000002843
Akshay Meena, Newshree Rout, Rajesh Nachiappa Ganesh, Sivaranjini Ramassamy

Abstract: A 20-year-old woman with acute myeloid leukemia (AML) with monocytic differentiation in remission presented with a recent onset painful indurated swelling on the tongue with fever. Although her peripheral blood picture was normal, the bone marrow biopsy was suggestive of a relapse of AML. A biopsy from the tongue lesion showed diffuse infiltration of lamina propria and submucosa by blast cells, positive for myeloperoxidase and CD11c and suggestive of oral myeloid sarcoma (MS). This presents an uncommon site of occurrence of MS and was a marker of relapse of AML. This case highlights the variable presentation of MS. It should prompt investigation for relapse of hematological malignancy in the bone marrow even in the absence of evidence from peripheral blood.

摘要:一名患有急性髓性白血病(AML)并伴有单核细胞分化的20岁女性患者,病情缓解后,最近出现舌头上疼痛性凹陷性肿胀,并伴有发热。虽然她的外周血象正常,但骨髓活检提示急性髓细胞白血病复发。舌病变活检显示,固有膜和粘膜下层弥漫性浸润有爆破细胞,髓过氧化物酶和 CD11c 阳性,提示为口腔髓系肉瘤(MS)。这是一种不常见的 MS 发病部位,也是急性髓细胞性白血病复发的标志。该病例凸显了 MS 的多变表现。即使在没有外周血证据的情况下,也应警惕骨髓中血液恶性肿瘤的复发。
{"title":"Oral Myeloid Sarcoma as a Marker of Relapse in Acute Myeloid Leukemia.","authors":"Akshay Meena, Newshree Rout, Rajesh Nachiappa Ganesh, Sivaranjini Ramassamy","doi":"10.1097/DAD.0000000000002843","DOIUrl":"https://doi.org/10.1097/DAD.0000000000002843","url":null,"abstract":"<p><strong>Abstract: </strong>A 20-year-old woman with acute myeloid leukemia (AML) with monocytic differentiation in remission presented with a recent onset painful indurated swelling on the tongue with fever. Although her peripheral blood picture was normal, the bone marrow biopsy was suggestive of a relapse of AML. A biopsy from the tongue lesion showed diffuse infiltration of lamina propria and submucosa by blast cells, positive for myeloperoxidase and CD11c and suggestive of oral myeloid sarcoma (MS). This presents an uncommon site of occurrence of MS and was a marker of relapse of AML. This case highlights the variable presentation of MS. It should prompt investigation for relapse of hematological malignancy in the bone marrow even in the absence of evidence from peripheral blood.</p>","PeriodicalId":50967,"journal":{"name":"American Journal of Dermatopathology","volume":"46 12","pages":"868-870"},"PeriodicalIF":1.1,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142683333","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}
引用次数: 0
期刊
American Journal of Dermatopathology
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