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Diagnostic Cytopathology最新文献

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Cytological diagnosis of lymphoepithelial carcinoma: Simple yet confusing. 淋巴上皮癌的细胞学诊断:简单却令人困惑。
IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-07-08 DOI: 10.1002/dc.25381
Shruti Gupta, Avinash Chandra Singh, Tanya Agarwal, Niraj Kumari, Arvind Rajwanshi

Lymphoepithelial carcinoma (LEC) of salivary glands are rare tumours and present as gradually progressing painless masses. LECs have good prognosis and accurate differentiation from secondary tumours and nasopharyngeal carcinoma is essential to dictate management. We present a case of an elderly male presenting with a parotid swelling diagnosed as LEC on fine needle aspiration cytology and confirmed on histopathology and immunohistochemistry.

唾液腺淋巴上皮癌(LEC)是一种罕见肿瘤,表现为逐渐进展的无痛性肿块。淋巴上皮癌预后良好,与继发性肿瘤和鼻咽癌的准确鉴别对治疗至关重要。我们报告了一例老年男性腮腺肿物病例,经细针穿刺细胞学检查确诊为 LEC,并经组织病理学和免疫组化检查确诊。
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引用次数: 0
Fine-needle aspiration cytology of diffuse type tenosynovial giant cell tumor with malignant trasformation and review of literature 弥漫型腱鞘巨细胞瘤伴恶性变形的细针穿刺细胞学检查和文献综述。
IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-06-24 DOI: 10.1002/dc.25338
Saba Shafi MD, William MacDonald MD, Swati Satturwar MD

Tenosynovial giant cell tumors (TGCTs) arise from the synovium of joint, bursa, and tendon sheath. Diffuse type often affects large joints, has higher recurrence rates, metastases, and malignant transformation potential compared to the localized type. The cytopathology of TGCT, a fibrohistiocytic neoplasm distinct from other giant cell–rich soft tissue tumors, is rarely reported. Here we describe cytomorphology of a case of TGCT that was initially diagnosed on fine-needle aspiration cytology (FNAC) consisting of a mixture of singly scattered polygonal or spindle mononuclear cells with hemosiderin laden macrophages, inflammatory cells, and a population of multinucleated osteoclast-like giant cells. Persistent symptoms and repeat excision were consistent with high-grade malignant transformation of the TGCT. Atypical cytologic features in a recurrent, infiltrative, or a metastatic lesion should raise suspicion for malignancy.

腱鞘巨细胞瘤(TGCT)产生于关节滑膜、滑囊和腱鞘。弥漫型常累及大关节,与局部型相比,复发率、转移率和恶变可能性更高。TGCT是一种有别于其他富含巨细胞的软组织肿瘤的纤维组织细胞肿瘤,其细胞病理学很少见报道。在此,我们描述了一例 TGCT 的细胞形态学,该病例最初经细针穿刺细胞学(FNAC)诊断为单个散在的多角形或纺锤形单核细胞与含血色素的巨噬细胞、炎性细胞和多核破骨细胞样巨细胞的混合物。持续的症状和重复切除与 TGCT 的高级别恶性转化一致。复发性、浸润性或转移性病变的非典型细胞学特征应引起对恶性肿瘤的怀疑。
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引用次数: 0
Urinary cytologic features of primitive neuroectodermal tumor primarily involving the kidney: A case report 主要累及肾脏的原始神经外胚层肿瘤的尿液细胞学特征:病例报告
IF 1.3 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-06-21 DOI: 10.1002/dc.25374
Kai Cheng, Xiaoxia Wang, Wei Bao, Rui Li, Xuan Wang, Qiu Rao
Renal primitive neuroectodermal tumor(rPNET) is an extremely rare and distinct entity that can be mistaken for a variety of other round cell tumors. Findings from fine needle aspiration cytology have been reported, but there have been no reports of PNET cytomorphological features in urine cytology specimen. Here, we report a case of PNET characterized by urine cytology. A 24‐year‐old girl presented with hematuria for half a month. Computed tomography showed a large tumor involving the upper pole of the right kidney. Urinary cytology exhibited highly cellular clusters composed of small, round, atypical cells with little cytoplasm and a high nuclear/cytoplasmic ratio. Following a right nephrectomy, the biopsy confirmed the diagnosis of rPNET. Additionally, immunohistochemistry (IHC) staining of the decolorized liquid‐based cytology slide was positive for CD99, further confirming the diagnosis through urine cytology. Our observations suggest that urinary cytology in combination with cytological morphology and immunocytochemistry may be a potentially useful method for the detection of PNET.
肾原始神经外胚层肿瘤(rPNET)是一种极为罕见的独特肿瘤,容易被误认为是其他各种圆形细胞肿瘤。细针穿刺细胞学检查结果已有报道,但尿液细胞学标本中的 PNET 细胞形态学特征尚未见报道。在此,我们报告了一例以尿液细胞学为特征的 PNET 病例。一名 24 岁女孩出现血尿半个月。计算机断层扫描显示右肾上极有一巨大肿瘤。尿液细胞学检查显示,肿瘤由小而圆的非典型细胞组成,细胞质少,核/质比例高。右肾切除术后,活检证实了 rPNET 的诊断。此外,脱色液基细胞学玻片的免疫组化(IHC)染色显示 CD99 呈阳性,进一步证实了尿液细胞学诊断。我们的观察结果表明,尿液细胞学结合细胞学形态学和免疫细胞化学可能是检测 PNET 的一种有效方法。
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引用次数: 0
EUS-FNA diagnosis of pancreatic tophaceous gout: Two rare cases 胰腺顶部痛风的 EUS-FNA 诊断:两例罕见病例
IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-06-17 DOI: 10.1002/dc.25323
Brant G. Wang MD, PhD, Iris H. Lee MD

We report two patients with pancreatic tophaceous gout diagnosed by endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) of presumed cystic mass lesions. The first case involved a patient who had a recent episode of acute pancreatitis 6 months prior, with subsequent imaging concerning for a pseudocyst or mass lesion. The second case involved a patient with epigastric pain associated with a pancreatic head cystic mass and an erroneous original diagnosis of a mucinous pancreatic neoplasm on EUS-FNA. Diff-Quik stained direct smears on fresh material obtained from EUS-FNA of the lesions showed chalky debris with needle shaped negatively birefringent crystals consistent with gout. For the first case, the chalky material was not present on the H&E stained paraffin embedded formalin fixed cellblock slides. The importance of inclusion of cytologic specimen preparations to examine monosodium urate crystals is emphasized.

我们报告了两名通过内镜超声引导下细针穿刺(EUS-FNA)诊断出假定囊性肿块病变的胰腺痛风患者。第一例患者在 6 个月前曾患急性胰腺炎,随后的影像学检查显示其为假性囊肿或肿块病变。第二例患者上腹部疼痛,伴有胰头囊性肿块,EUS-FNA 原始诊断为粘液性胰腺肿瘤。从 EUS-FNA 病变部位获得的新鲜材料经 Diff-Quik 染色后直接涂片,显示出白垩状碎屑和针状负双折射结晶,与痛风一致。第一个病例的 H&E 染色石蜡包埋福尔马林固定细胞块切片上没有白垩状物质。强调了细胞学标本制备对检查单钠尿酸盐结晶的重要性。
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引用次数: 0
Pulmonary Kaposi sarcoma in a patient with bilateral lung transplant: An unexpected diagnosis on transbronchial fine needle aspiration and core biopsy 一名双肺移植患者的肺卡波西肉瘤:经支气管细针穿刺和核心活检的意外诊断。
IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-06-11 DOI: 10.1002/dc.25368
Levent Trabzonlu MD, Shaunagh McDermott MBBCH, BAO, Martha B. Pitman MD, Ivan Chebib MD

Kaposi sarcoma (KS) is a low-grade vascular neoplasm that can be seen in various sites, most commonly seen in skin and mucosal tissues. Cytologic features of KS have been well-documented in the literature, however, since it is rarely seen in visceral organs, it could pose significant diagnostic challenges on fine needle aspiration (FNA) biopsies. We present a case of pulmonary KS diagnosed on transbronchial FNA biopsy in a 70-year-old female bilateral lung allograft recipient 11 months after transplantation. The aspirate smears showed a moderately cellular specimen containing a mixture of small, tightly cohesive clusters and loosely clustered groups of monomorphic, ovoid to spindled cells with moderate nuclear to cytoplasmic ratio. An extensive immunohistochemical panel on the concurrent core biopsy showed the tumor cells to be positive for ERG, KIT, and HHV8, confirming the diagnosis. We compared our case to previously published reports of confirmed pulmonary KS in lung allograft recipients.

卡波西肉瘤(KS)是一种低级别血管肿瘤,可见于不同部位,最常见于皮肤和粘膜组织。KS的细胞学特征在文献中已有详细记载,但由于其很少见于内脏器官,因此可能会给细针穿刺活检(FNA)的诊断带来巨大挑战。我们报告了一例经支气管 FNA 活检确诊的肺 KS 病例,患者是一名 70 岁的女性双侧肺异体移植受者,移植后 11 个月。吸出物涂片显示标本中度蜂窝状,包含由单形、卵圆形至纺锤形细胞组成的小而紧密的团块和松散的团块混合物,细胞核与细胞质比例适中。对同时进行的核心活检进行的广泛免疫组化检查显示,肿瘤细胞的ERG、KIT和HHV8均呈阳性,从而确诊了这一病例。我们将本病例与之前发表的肺移植受者肺KS确诊报告进行了比较。
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引用次数: 0
Endobronchial ultrasound-guided transbronchial fine needle aspiration of mediastinal lymphadenopathy: Diagnostic performance and clinical implications of the World Health Organization reporting system 支气管内超声引导下经支气管细针穿刺纵隔淋巴结病:世界卫生组织报告系统的诊断性能和临床意义。
IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-06-09 DOI: 10.1002/dc.25365
Kajsa Ericson Lindquist MD, PhD, Gaêlle Cortas MS, Yas Hashemi MS, Nilofar Rajabian MD, Mats Ehinger MD, PhD

Introduction

Lymph node fine-needle aspiration cytology (LN-FNAC) is a common, rapid, minimally invasive and cost-effective diagnostic method. For mediastinal lymph nodes, endobronchial ultrasound (EBUS) guided LN-FNAC is a first-line investigation and has an indispensable role in the diagnosis and staging of patients with suspected lung cancer. Recently, a new WHO system has been proposed for classification of LN-FNAC heralding five different diagnostic categories; insufficient, benign, atypical, suspicious for malignancy and malignant. The aim of this study was to evaluate the diagnostic accuracy and risk of malignancy (ROM) of these categories in EBUS-guided LN-FNAC from mediastinal lymph nodes.

Method

We evaluated 2110 consecutive mediastinal lymph nodes during this one-year retrospective study. Corresponding radiological images and histologic material were used as ground truth to calculate accuracy, sensitivity, specificity and ROM.

Results

The WHO system showed an overall accuracy of 93.7% with a sensitivity of 83.0% and a specificity of 97.5%. The positive predictive value was 92.3% and the negative predictive value 94.2%. The overall ROM for each category in the WHO classification system was 12.8% for the inadequate, 2.4% for the benign, 47.4% for the atypical, 81.0% for the suspicious for malignancy and 93.6% for the malignant category.

Conclusion

The results of the present study indicate that the new WHO system entails a high diagnostic accuracy regarding EBUS-guided LN-FNAC assessment of mediastinal lymph nodes and supports its integration into clinical practice. Application of the WHO system standardizes risk assessment thus facilitating communication between cytopathologists and clinicians and minimizes the need for histopathological analysis.

简介淋巴结细针穿刺细胞学检查(LN-FNAC)是一种常见、快速、微创且经济有效的诊断方法。对于纵隔淋巴结,支气管内超声(EBUS)引导的淋巴结细针穿刺细胞学检查是一线检查方法,在疑似肺癌患者的诊断和分期中发挥着不可或缺的作用。最近,世界卫生组织提出了一种新的 LN-FNAC 分类系统,预示着五种不同的诊断类别:不足、良性、非典型、恶性可疑和恶性。本研究旨在评估 EBUS 引导下纵隔淋巴结 LN-FNAC 诊断类别的准确性和恶性风险(ROM):在这项为期一年的回顾性研究中,我们对 2110 个连续纵隔淋巴结进行了评估。以相应的放射影像和组织学材料为基础,计算准确性、敏感性、特异性和ROM:世卫组织系统的总体准确率为 93.7%,灵敏度为 83.0%,特异度为 97.5%。阳性预测值为 92.3%,阴性预测值为 94.2%。WHO分类系统中每个类别的总体ROM分别为:不充分类12.8%、良性类2.4%、不典型类47.4%、恶性可疑类81.0%和恶性类93.6%:本研究结果表明,新的 WHO 系统对 EBUS 引导的纵隔淋巴结 LN-FNAC 评估具有很高的诊断准确性,并支持将其纳入临床实践。WHO系统的应用使风险评估标准化,从而促进了细胞病理学家和临床医生之间的交流,并最大限度地减少了组织病理学分析的需要。
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引用次数: 0
HER2-positive mucinous cystadenocarcinoma of the breast coexisting with invasive lobular carcinoma: A case report and review of the literature HER2阳性乳腺粘液性囊腺癌与浸润性小叶癌并存:病例报告和文献综述。
IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-06-04 DOI: 10.1002/dc.25364
Ismail Guzelis MD, Betul Bolat Kucukzeybek MD, PhD, Mehmet Ali Uyaroglu MD, Melek Bekler Gokova MD, Gulten Sezgin MD, Yuksel Kucukzeybek MD

Primary mucinous cystadenocarcinoma (MCA) of the breast is a rare variant of breast carcinoma. A 68-year-old female patient presented to the general surgery clinic with pain and swelling in the right breast. A mass was detected in the upper outer quadrant, and a fine-needle aspiration biopsy was performed. The May-Grünwald Giemsa stained slides showed aggregates of mucin-rich pleomorphic cells with large nuclei in a mucinous background containing discohesive single cells. The Papanicolaou stain revealed a papillary structure composed of malignant epithelial cells in a necrotic background. A modified radical mastectomy was performed, and upon gross examination, two tumors were discovered in the central and upper outer quadrants. The first tumor, located centrally, was identified as invasive lobular breast carcinoma. The second tumor was an MCA with cytokeratin 7(+) and cytokeratin 20(−), and was determined to be the primary MCA of the breast based on clinical and radiological information. Immunohistochemistry revealed that the tumor cells were negative for estrogen receptor and progesterone receptor, and HER2 was 2+. Fluorescence in situ hybridization analysis detected HER2 gene amplification. During the 72-month follow-up, there were no findings compatible with recurrence or new metastasis. Although primary MCA is rare, it causes differential diagnosis problems and has different biological behaviors.

乳腺原发性粘液囊腺癌(MCA)是乳腺癌的一种罕见变异。一名 68 岁的女性患者因右侧乳房疼痛和肿胀来到普外科门诊就诊。在外侧上象限发现一个肿块,于是进行了细针穿刺活检。May-Grünwald Giemsa 染色切片显示,在含有盘状单细胞的粘液背景中,富含粘蛋白的多形性细胞聚集,核较大。巴氏染色显示,乳头状结构由坏死背景中的恶性上皮细胞组成。患者接受了改良根治性乳房切除术,经大体检查,在中央和外上象限发现了两个肿瘤。第一个肿瘤位于中心位置,被确定为浸润性乳腺小叶癌。第二个肿瘤是一个细胞角蛋白7(+)和细胞角蛋白20(-)的MCA,根据临床和放射学信息确定为乳腺原发性MCA。免疫组化显示,肿瘤细胞的雌激素受体和孕激素受体阴性,HER2为2+。荧光原位杂交分析检测到 HER2 基因扩增。在 72 个月的随访中,没有发现复发或新的转移。原发性 MCA 虽然罕见,但会造成鉴别诊断问题,而且具有不同的生物学行为。
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引用次数: 0
Process improvement in thyroid fine needle aspiration: Standardizing number of smears for enhanced adequacy and diagnosis 甲状腺细针穿刺的流程改进:标准化涂片数量,提高充分性和诊断率。
IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-06-03 DOI: 10.1002/dc.25360
Patrick Morse MD, Kaleigh F. Roberts MD, PhD, Nicholas C. Spies MD, Vijayalakshmi Padmanabhan MPH, MBBS

Fine-needle aspiration (FNA) is a safe, cost-effective diagnostic procedure used in the evaluation of thyroid nodules. The number of thyroid FNAs has dramatically increased over the past few years. In the absence of standardized procedures regarding the number of needle passes needed for diagnosis and the lack of clarity on the use of conventional smears (CS) versus liquid-based preparations (LBP), the demand of thyroid FNAs has led to increased workload on cytology laboratories, which can negatively affect patient safety. We implemented a standardized two needle passes for CS and collection of all needle rinses and additional pass material in CytoRich Red for ThinPrep LBP and compared the non-diagnostic and diagnostic rates before and after this intervention. There were 290 pre-intervention cases and 348 post-intervention cases; of which, there were 17 (5.9%) non-diagnostic cases of the pre-intervention group and 27 (7.8) non-diagnostic cases of the post-intervention group. There was no statistically significant difference in non-diagnostic and diagnostic rates before and after the change (p = 0.347 by two-tailed Z test).

细针穿刺术(FNA)是用于评估甲状腺结节的一种安全、经济有效的诊断方法。在过去几年中,甲状腺 FNA 的数量急剧增加。由于缺乏诊断所需穿刺针数的标准化程序,以及传统涂片(CS)与液基制剂(LBP)的使用方法不明确,甲状腺 FNA 的需求导致细胞学实验室的工作量增加,从而对患者的安全产生了负面影响。我们对 CS 实施了标准化的两针穿刺,并收集了 ThinPrep LBP 的所有针头冲洗液和额外的穿刺材料CytoRich Red,比较了干预前后的非诊断率和诊断率。干预前有 290 例,干预后有 348 例;其中干预前组有 17 例(5.9%)未诊断,干预后组有 27 例(7.8%)未诊断。干预前后的非诊断率和诊断率在统计学上没有显著差异(经双尾 Z 检验,P = 0.347)。
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引用次数: 0
A case of metastatic HPV-related cervical small cell neuroendocrine carcinoma with varying cytomorphology found in cytological specimens of a solid organ transplant recipient 一例在实体器官移植受者的细胞学标本中发现的细胞形态各异的转移性人乳头瘤病毒相关宫颈小细胞神经内分泌癌。
IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-05-31 DOI: 10.1002/dc.25361
Henrietta Fasanya-Maku MD, PhD, Danielle Petty DO, Jaquelyn Knapik MD, Marino Leon MD, Catherine Gonsalves MD

Small cell neuroendocrine carcinoma (NEC) of the cervix is a rare gynecological malignancy, constituting 2%–5% of all such cases. As high-risk Human Papilloma Virus (HR-HPV) infections contribute to 85% of these tumors, small cell NEC poses a significant risk for solid organ transplant recipients, increasing their risk of progressive disease. We present a case of an uterine cervix small cell NEC with metastasis to the bladder and pleural cavities in a 53-year-old woman with a past medical history of kidney transplantation, who presented with abnormal uterine bleeding. The initial liquid preparation (ThinPrep) cytology stained with Papanicolaou (Pap) showed an adenocarcinoma not otherwise specified. At the time of diagnosis, the patient had diffusely metastatic disease. A subsequent uterine cervix biopsy was consistent with a small cell NEC. Despite treatment with chemotherapy, the patient's condition deteriorated, evidenced by a worsening right-sided pleural effusion one-month postdiagnosis. A pleural effusion showed a tumor with glandular features, with immunohistochemistry suggestive of metastatic adenocarcinoma. HR HPV E6/E7 RNA in situ hybridization (ISH) was positive. Bladder washing showed cytopathologic findings consistent with bladder involvement by small cell carcinoma. The patient's lesions in both urine and pleural fluids showed distinct cytomorphology. Within a year of diagnosis, the patient was declared deceased. This case highlights the existence of carcinoma admixed with NEC tumor, such as an HPV associated adenocarcinoma admixed with a NEC and underscores the elevated risk of HPV-related genital lesions in renal transplant patients. In patients with a history of solid organ transplant or other immunosuppressive conditions, there is an increased necessity for enhanced surveillance and appropriate cancer screening.

宫颈小细胞神经内分泌癌(NEC)是一种罕见的妇科恶性肿瘤,占所有此类病例的 2%-5%。由于高危人类乳头状瘤病毒(HR-HPV)感染导致了85%的此类肿瘤,因此小细胞NEC对实体器官移植受者构成了重大风险,增加了他们罹患进展性疾病的风险。我们报告了一例子宫颈小细胞 NEC 并转移至膀胱和胸膜腔的病例,患者是一名 53 岁的女性,既往有肾移植病史,并伴有异常子宫出血。经巴氏染色的初始液体制备(ThinPrep)细胞学检查显示为未特殊说明的腺癌。确诊时,患者已出现弥漫性转移。随后的子宫颈活检结果与小细胞 NEC 一致。尽管接受了化疗,但患者的病情仍在恶化,确诊后一个月出现的右侧胸腔积液就是证明。胸腔积液显示肿瘤具有腺体特征,免疫组化提示为转移性腺癌。HR HPV E6/E7 RNA原位杂交(ISH)呈阳性。膀胱冲洗显示细胞病理学结果与小细胞癌累及膀胱一致。患者尿液和胸腔积液中的病变均显示出明显的细胞形态学特征。确诊后不到一年,患者宣告死亡。该病例强调了NEC肿瘤中混杂癌的存在,如NEC中混杂HPV相关腺癌,并强调肾移植患者发生HPV相关生殖器病变的风险较高。对于有实体器官移植史或其他免疫抑制病史的患者,更有必要加强监测和适当的癌症筛查。
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引用次数: 0
Response to commentary on “Benchtop fine needle aspirations: An untapped source of cytologic educational material” 对 "台式细针抽吸术:尚未开发的细胞学教材来源 "的评论。
IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-05-30 DOI: 10.1002/dc.25363
Yubo Wu MD, Marcos Lepe MD
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引用次数: 0
期刊
Diagnostic Cytopathology
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