excision biopsy

  • 文章类型: Case Reports
    纤维瘤是毛囊的良性结缔组织肿瘤,通常表现为头颈部的多发性病变。孤立性纤维囊瘤是一种罕见的实体,以前在than区没有描述过。作者报告了一例不寻常的病例,一名43岁的女性在切除活检后被发现有一个孤立的纤维囊瘤,位于内侧can附近。虽然罕见,在眼睑病变的鉴别诊断中应考虑纤维囊瘤。
    Fibrofolliculomas are benign connective tissue tumours of the hair follicle that typically present as multiple lesions over the head and neck. A solitary fibrofolliculoma is a rare entity and has not been previously described in the canthal region. The authors report an unusual case of a 43-year-old female who was found to have a solitary fibrofolliculoma located in close proximity to the medial canthus following an excision biopsy. Whilst rare, fibrofolliculomas should be considered in the differential diagnosis of an eyelid lesion.
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  • 文章类型: Case Reports
    鳞状乳头状瘤是良性的,外生性,由分层鳞状上皮的快速增殖引起的软组织肿瘤。它通常在口腔中表现为无痛,软,非招标,像花椰菜的有花序梗的生长。此例硬腭鳞状乳头状瘤的报告揭示了其病因。类型,临床特征,鉴别诊断,和管理方式。
    Squamous papilloma is a benign, exophytic, soft tissue tumour caused by the rapid proliferation of stratified squamous epithelium. It typically manifests in the oral cavity as a painless, soft, non-tender, pedunculated growth that resembles a cauliflower. This case report of squamous papilloma on the hard palate sheds light on the etiopathogenesis, types, clinical features, differential diagnosis, and management modalities.
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  • 文章类型: Case Reports
    未经证实:尽管上肢肌内血管瘤是一种罕见的临床实体,它在个体的功能需求中造成相当大的发病率。肌内血管瘤的诊断存在诊断故障。联合的放射学和组织病理学评估为其提供了完整的理解和诊断。每个肿瘤都遵循个体化的治疗方案。
    未经证实:一名15岁女性,出现右前臂远端1/3背侧肿胀,在过去的5年中,距离右手腕关节面3厘米。右手腕无外伤或感染史。Finkelstein的测试是阴性的,排除了德·克尔文的腱鞘炎。右手腕的运动不受限制,没有任何远端神经血管缺陷。她的右手腕和手的MRI提示APL和EPB肌的肌肌腱交界处存在低流量血管畸形。患者接受了血管瘤性病变的切除活检,没有任何神经系统并发症。随访6个月无复发。
    未经批准:是良性血管肿瘤,MRI为诊断肌内血管瘤提供了途径,以便早期干预以提供更好的功能结果。APL和EPB血管瘤的明确治疗方法的选择是切除活检,从而为我们的患者提供更好的功能结果。
    UNASSIGNED: Although upper extremity intramuscular hemangioma is a rare clinical entity, it poses considerable morbidity in the functional needs of an individual. The diagnosis of intramuscular hemangioma poses a diagnostic glitch. The combined radiological and histopathological assessment provides a complete understanding and diagnosis for the same. Every tumor follows an individualized protocol for its management.
    UNASSIGNED: A 15-year-old female presented with swelling over dorsal aspect of distal 1/3rd right forearm, which was 3 cm away from the articular surface of the right wrist from the past 5 years. There was no history of trauma or infection over the right wrist. Finkelstein\'s test was negative, which rule out de Quervain\'s tenosynovitis. The movements of the right wrist were unrestricted without any distal neurovascular deficit. MRI of her right wrist and hand suggested the presence of low flow vascular malformation within the musculotendinous junction of APL and EPB muscles. The patient underwent excision biopsy of the hemangiomatous lesion in toto without any neurological complications. No recurrence was noted in the follow-up period for 6 months.
    UNASSIGNED: Being a benign vascular tumor, MRI provides the gateway to diagnose intramuscular hemangioma for early intervention to provide better functional results. The choice of definitive treatment for APL and EPB hemangioma was excision biopsy in toto which provided better functional results in our patient.
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  • 文章类型: Case Reports
    乳腺纤维瘤病是一种罕见的软组织病变,由乳腺组织或胸筋膜引起。我们介绍了一名39岁男性患者的纤维瘤病病例,该患者在几周内没有经过外伤或手术就出现了右外侧乳房肿块。超声引导下的核心针活检结果包括结节性筋膜炎和纤维瘤病的鉴别诊断。患者被转诊给乳腺外科医生,并接受了切除活检。最终病理报告证实纤维瘤病。患者对手术的耐受性良好,术后将继续随访复发。
    Fibromatosis of the breast is a rare soft tissue lesion that arises from the mammary tissue or the pectoral fascia. We present a case of fibromatosis in a 39-year-old male patient who developed a right lateral breast mass in several weeks without prior trauma or surgery. Ultrasound-guided core needle biopsy findings included differential diagnoses of nodular fasciitis and fibromatosis. The patient was referred to a breast surgeon and underwent excisional biopsy. Final pathology report confirmed fibromatosis. The patient tolerated the surgery well and will continue to follow up post-operatively for recurrence.
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  • 文章类型: Case Reports
    背景:滑膜内血管瘤,一种罕见的关节腔良性血管病变,也称为滑膜内乳头状内皮增生或Masson血管瘤(MH)。这些病变的特征是内皮细胞异常增殖,轻度异型性伴有有组织的血栓。MH遵循个性化的管理协议。
    方法:一名22岁男性患者有10年的左膝滑膜血管瘤诊断和手术史(关节镜),并有类似的主诉。左膝无外伤或感染史。除了运动的末端限制外,左膝盖的运动是正常的。左膝MRI提示滑膜物质内滑膜内低流量血管畸形。该患者在8个月的随访期内对血管瘤性病变进行了滑膜切除术,无任何复发。组织病理学证实诊断为血管内乳头状内皮增生/MH。
    结论:虽然滑膜内血管瘤是一种非常罕见的临床实体,骨科医生应该对MH有很高的怀疑指数,当在临床实践中遇到长期的膝关节疼痛和关节积血时。
    BACKGROUND: Intrasynovial hemangioma, a rare benign vascular lesion of joint cavities, is also called intrasynovial papillary endothelial hyperplasia or Masson\'s hemangioma (MH). These lesions are characterized by abnormal proliferation of endothelial cells with mild atypia with an organized thrombus. MH follows an individualized protocol for its management.
    METHODS: A 22-year-old male gave a 10-year history of the diagnosed and operated (arthroscopically) case of synovial hemangioma of the left knee and presented with similar complaints. There was no history of trauma or infection over the left knee. The movements of the left knee were normal except with terminal restriction of movements. MRI of the left knee suggested intrasynovial low flow vascular malformation within the substance of the synovium. The patient underwent synovectomy of the hemangiomatous lesion in toto without any recurrence in the follow-up period for 8 months. Histopathology confirmed the diagnosis of intravascular papillary endothelial hyperplasia/MH.
    CONCLUSIONS: Although intrasynovial hemangioma is a very rare clinical entity, Orthopedic surgeons should have a high index of suspicion for MH, when a long-standing pain and hemarthrosis of the knee joint is being encountered in the clinical practice.
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  • 文章类型: Journal Article
    BACKGROUND: Fibroadenomas (FAs) and phyllodes tumors (PTs) are less prevalent but allied to have malignant transformation in many instances. It is a challenge to diagnose the phyllodes by conventional trucut biopsy technique.
    OBJECTIVE: To evaluate the histological characteristics of tumors labeled as fibroepithelial lesions of breast tissues on trucut biopsy and compare with a diagnosis on excision biopsy.
    METHODS: It was a descriptive cross-sectional study that was carried out in Shaukat Khanum Memorial Hospital and Research Centre within six years from January 2015 to January 2021. In trucut samples, stromal cellularity, stromal cell nuclear atypia, mitotic count, stromal overgrowth, the enhancement of stromal cellularity adjacent to epithelium were scrutinized. In each category, the activity was seen as absent, mild, moderate, or severe. Mitotic activity was graded as 0-1, 0-5, 5-10, >10.
    RESULTS: A total of 125 patients were registered for the study. The mean age of patients in our study was 33.86 ± 9.95 years. The mean size was 41.02 ± 27.38 mm with a mean lump duration of 7.52 ± 5.34 months. In the FA group, the trucut sampling report showed the stromal cellularity as mild in 62 (69.7%) and stromal cell nuclear atypia as absent in 68 (76.4%) cases. But in the phyllodes tumor group, the stromal cellularity was severe in 10 (27.8%) patients and stromal cell nuclear atypia was severe in five (13.9%). The ultimate outcome showed that 89 (71.2%) patients had FA and 36 (28.8%) had PT at excision.
    CONCLUSIONS: Assessment of tumor size, stromal cellularity, mitoses, and enhancement of stromal cellularity adjacent to epithelium are useful markers for diagnosing the PT in trucut needle biopsy.
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  • 文章类型: Journal Article
    BACKGROUND: The management of complex cysts of the breast is an ongoing topic of discussion. The aim of this study was to determine the prevalence of underlying malignancy in radiologically diagnosed complex cysts, and to assess whether watchful waiting could be the preferred method to safely manage complex cysts of the breast.
    METHODS: A single-center retrospective study was performed between May 2003 and November 2019 in the VieCuri Medical Centre. Women with a radiologically diagnosed complex cyst of the breast were included. Prevalence of underlying malignancy was calculated, as were absolute risk reduction and number needed to treat in order to diagnose malignancy. In addition, patient characteristics were compared to determine characteristics associated with malignancy.
    RESULTS: Of 78 radiologically diagnosed complex cysts of the breast, five (6,4%) were found to be malignant. The number needed to treat was calculated at 12,8 (absolute riks reduction 0,078). Age (P = 0,003) was associated with malignancy.
    CONCLUSIONS: Complex cysts of the breast could be managed more conservatively. Patient characteristics can be used to assess the eligibility for radiological follow-up. This, in turn, would lead to a lower NNT and possibly a decrease in disease burden and healthcare costs.
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  • 文章类型: Case Reports
    The intramuscular hemangioma is a rare clinical entity in the upper extremity. Pronator quadratus hemangioma poses a considerable morbidity in the functional quality of life of an individual. MRI remains the gold standard modality in diagnosing this rare entity. Additionally, histopathological examination of the lesion corroborates for the same. PQH follows an individualized protocol in the management of the tumour. A 35-year-old female presented with pain over her right wrist from past 1 year which was dull aching, non-radiating, localised to the palmar aspect of distal 1/3rd of the right forearm. There was no history of trauma or infection over the right wrist. Swelling was present over the palmar aspect of distal 1/3rd of right forearm, which was non-pulsatile, non-fluctuant, non-transilluminant, non-compressible, non-reducible and skin over the swelling was pinchable. The movements of the right wrist were painful and restricted. There was no distal neurovascular deficit. The MRI of her right wrist and hand suggested the presence of low flow vascular malformation within pronator quadratus muscle. The patient underwent excision biopsy of pronator quadratus in toto without any neurological complications. No recurrence was noted in the follow-up period for 12 months. The pronator quadratus hemangioma is a rare clinical entity where the natural course of disease and pathophysiology remains controversial. MRI serves as the gold standard in the diagnosis of intramuscular hemangioma. The management of such tumour has to be individualized based on the functional needs of the patient. The natural course of the disease has to be elicited to decrease the morbidity and enhance the functional quality of life of the patient.
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  • 文章类型: Journal Article
    在丹麦,细针抽吸是从颈部淋巴结(LN)获取组织样本的标准化工具。然而,因为对淋巴瘤的特异性低,怀疑这种疾病的LN通常通过手术切除和检查。国际研究表明,芯针活检(CNB)足以检测淋巴瘤,从而有可能避免手术。然而,所有研究都是回顾性研究,这项前瞻性研究的目的是发现CNB的真正敏感性.
    57名患者被纳入研究,由于缺乏CNB材料而被排除在外。怀疑淋巴瘤的LN被手术从颈部切除,此后,从除去的LN获得CNB。CNB和LN的剩余部分被送到病理学部门进行进一步处理,并且样品被致盲并分别由两名病理学家检查。在诊断建议不同的情况下,达成了共识诊断。计算了CNB方法与整个组织切片相比用于淋巴瘤诊断的敏感性。
    CNB方法在66%的淋巴瘤病例中给出了正确的诊断,14%的患者没有定论,18%的患者给出了不正确的淋巴瘤亚型。2%的CNB错误地导致良性诊断。CNB在所有非淋巴瘤病例中是正确的;从而保持100%的特异性。
    这项前瞻性研究发现,用CNB诊断淋巴瘤的敏感性为66%。由于本研究中的CNB是在最佳条件下获得的,与临床实践不同,我们得出的结论是,CNB不能被推荐作为诊断淋巴瘤的标准工具。
    UNASSIGNED: In Denmark, fine needle aspiration is the standardized tool for obtaining tissue samples from lymph nodes (LN) of the neck. However, because of a low specificity toward lymphomas, LNs suspicious for this disease are often surgically removed and examined. International studies have implied that a core needle biopsy (CNB) is sufficient for detecting lymphomas, thereby potentially avoiding surgery. However, all studies have been conducted retrospectively and the goal of this prospective study was to find the true sensitivity of CNB.
    UNASSIGNED: Fifty-seven patients were enrolled in the study, one was excluded due to lack of CNB material. LNs suspected for lymphoma were surgically removed from the neck, whereafter a CNB was obtained from the removed LN. The CNB and the remaining part of the LN were sent to the Department of Pathology for further processing and the samples were blinded and examined by two pathologists separately. A consensus diagnosis was reached in cases with divergent diagnostic proposals. Sensitivity of the CNB method in comparison to whole tissue sections for lymphoma diagnosis was calculated.
    UNASSIGNED: The CNB method gave the correct diagnosis in 66% of lymphoma cases, was inconclusive in 14% and gave an incorrect lymphoma subtype in 18%. In 2% the CNB wrongly resulted in a benign diagnosis. CNB was correct in all the non-lymphoma cases; thereby retaining a specificity of 100%.
    UNASSIGNED: This prospective study found a sensitivity of 66% for diagnosing lymphoma with a CNB. As the CNB in this study was obtained under optimal conditions, unlike in clinical practice, we conclude that CNB cannot be recommended as a standard tool for diagnosing lymphomas.
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  • 文章类型: Evaluation Study
    BACKGROUND: We evaluated the use and value of breast surgical excision biopsies for diagnostic purposes over the last decades in women undergoing mammographic screening, either as a primary procedure or following an inconclusive percutaneous biopsy.
    METHODS: All women with an excision biopsy among 817,656 screens, obtained from January 1997 to January 2017, were included.
    RESULTS: Of 18,593 recalled women (recall rate, 2.3%) with screen-detected abnormalities, 908 (4.9%) underwent excision biopsy. Of these, 411 (45.3%) were performed as first diagnostic intervention, decreasing from 4.3 per 1000 screens in 1997-1998 to 0 per 1000 screens in 2015-2016. The remaining 497 (54.7%) excision biopsies were performed secondary to pathologic findings at percutaneous biopsy. During 1997-1998, 1.0 secondary biopsies per 1000 screens were performed, decreasing to 0.3 per 1000 in 2005-2006 and afterwards increased to 0.6 per 1000 in 2015-2016 (p = 0.003). Of all 487 secondary biopsies, 303 (61.0%) had a benign pathology outcome, increasing from 40.4% in 1997-1998 to 70.2% in 2015-2016. Of all 211 biopsies in the three most recent cohorts (2011-2016) the overall upgrade rate was 26.5%, consisting of 39 (18.5%) DCIS (27 low grade) and 17 (8.1%) invasive carcinomas.
    CONCLUSIONS: Although the use of excision biopsy significantly decreased over the past two decades, we observed a significant increased rate in more recent years. Since the vast majority of currently performed excision biopsies reveals a benign diagnosis or shows low grade DCIS, a secondary excision biopsy should only be considered if radiologic surveillance and repeated percutaneous biopsy continues to yield indeterminate results.
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