MDT

MDT
  • 文章类型: Case Reports
    肺泡横纹肌肉瘤是一种严重恶性软组织肉瘤,主要影响儿童和青少年。然而,在这种肿瘤导致上肢局部骨破坏的情况下,医学领域缺乏关于最佳手术方法的共识。
    一名17岁男性左前臂有肿块,CT和MRI显示肿块穿透尺骨皮质,浸润髓质,导致形成偏心的跨心室肿瘤病灶。相当大的肿瘤影响了前臂的掌侧肌肉以及尺骨骨髓,对尺动脉和静脉施加压力。穿刺活检证实肿块为肺泡横纹肌肉瘤。经过两个疗程的新辅助化疗,肿瘤被广泛切除。在手术过程中,使用带有血管蒂的自体腓骨进行重建。在术后随访中,未观察到肿瘤局部复发.此外,患者在左前臂保留了令人满意的腕关节屈曲和内旋功能。
    肺泡横纹肌肉瘤是一种罕见且高度侵袭性的软组织肉瘤。科学管理需要多学科的方法,化疗与手术相结合。如果肿瘤侵入骨腔,应该仔细考虑肿瘤切除的边界,截骨的范围,以及设计手术计划时肌肉骨骼重建的方法。通过报告我们自己的病例并彻底回顾以前的临床经验,我们旨在为这种特殊疾病的治疗提供有价值的见解。
    UNASSIGNED: Alveolar Rhabdomyosarcoma is a profoundly malignant soft-tissue sarcoma that predominantly affects children and adolescents. However, the medical field lacks consensus regarding the optimal surgical approach to be undertaken in cases where this tumor causes local bone destruction in the upper limb.
    UNASSIGNED: A 17-year-old male presented a mass in his left forearm and CT and MRI indicated that the mass had penetrated the ulnar cortex and infiltrating the medulla, resulting in the formation of an eccentric trans-ventricular tumor focus. The sizable tumor affected the volar muscles of the forearm as well as the ulnar bone marrow, exerting pressure on the ulnar artery and vein. It was confirmed by needle biopsy that the mass is alveolar rhabdomyosarcoma. Following two courses of neoadjuvant chemotherapy, the tumor was widely excised en bloc. Autologous fibula with a vascular pedicle was utilized for reconstruction during the procedure. In the postoperative follow-up, no local recurrence of the tumor was observed. Furthermore, the patient retained satisfactory wrist flexion and pronation function in the left forearm.
    UNASSIGNED: Alveolar rhabdomyosarcoma is an uncommon and highly aggressive form of soft tissue sarcoma. Scientific management necessitates a multidisciplinary approach, combining chemotherapy with surgery. In cases where the tumor invaded into compartment of the bone, careful consideration should be given to the boundaries of tumor resection, the extent of osteotomy, and the approach to musculoskeletal reconstruction when designing the surgical plan. Through reporting our own case and thoroughly reviewing previous clinical experiences, we aim to provide valuable insights for the treatment of this particular disease.
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  • 文章类型: Case Reports
    我们报告一例新生儿Carmi综合征。
    分享我们在Carmi综合征病例诊断方面的经验教训。
    Carmi综合征是一种极其罕见的常染色体隐性遗传病,其特征是幽门闭锁和交界性大疱性表皮松解症并存,大约28%的患者患有先天性皮肤发育不全。在这种情况下,一名足月男性新生儿在医院通过剖宫产分娩出生到G4P2+1L1经产妇,与4000mLII°胎粪染色羊水非血缘婚姻.他被发现小腿和其他部位大面积皮肤脱落,有分散的水疱和双侧小耳畸形。腹部X线平片显示胃气泡大,远端无气体。由于未知原因,母亲先前有宫内胎儿丢失。皮肤科医生诊断新生儿患有巴特综合症,而儿科外科医生诊断为先天性幽门闭锁(CPA)。父母拒绝进一步治疗,新生儿在出生后约30小时去世。
    新生儿出生后约30小时死亡。
    这个案例的教训:①。排除PA患者的Carmi综合征,并区分Bart综合征和Carmi综合征患者的皮肤异常表现。②.对于罕见和/或严重的疾病,应建立多学科小组(MDT)。③.在随后的生育之前,遗传咨询和产前诊断是必要的。④.如果发现某些指标,则可以考虑终止妊娠。
    UNASSIGNED: We report a case of Carmi Syndrome in a neonate.
    UNASSIGNED: To share our lessons in diagnosis of the case of Carmi Syndrome.
    UNASSIGNED: Carmi Syndrome is an extremely rare autosomal recessive genetic disorder characterized the coexistence of pyloric atresia and junctional epidermolysis bullosa, and with aplasia cutis congenita in approximately 28% patients. In this case, a full-term male neonate was born to a G4P2+1L1 multipara through cesarean section delivery in hospital in a non-consanguineous marriage with 4000mL of II°meconium-stained amniotic fluid. He was found extensive skin loss over lower legs and other parts, with scattered blisters and bilateral microtia. Plain abdominal X-ray revealed a large gastric air bubble with no gas distally. The mother had an intrauterine fetal loss previously for reasons unknown. The dermatologist diagnosed the newborn with Bart Syndrome, while the pediatric surgeon diagnosed congenital pyloric atresia(CPA). The parents refused further treatment and the neonate passed away about 30 hours after birth.
    UNASSIGNED: The neonate passed away about 30 hours after birth.
    UNASSIGNED: Lessons from this case:①.Rule out Carmi Syndrome in patients with PA, and differentiate Bart syndrome and Carmi Syndrome in patients with abnormal skin manifestations. ②. For rare and/or severe diseases, multidisciplinary teams(MDTs) should be establish. ③. Genetic counseling and prenatal diagnosis are necessary prior to subsequent childbearings. ④.Termination of pregnancy might be contemplated if certain indicators are revealed.
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  • 文章类型: Case Reports
    乳腺癌和非霍奇金淋巴瘤的同时发生是一种罕见的疾病,具有诊断和治疗挑战。先前尚未描述滤泡性淋巴瘤(FL)和三阴性乳腺癌(TNBC)的共存。
    一个46岁的女人,已经遭受了未经治疗的历史,高级阶段,高肿瘤负荷FL,因快速进展的右乳房肿块入院。超声检查显示右乳有8.3×3.6×4.1cm的基底肿块,双侧腋窝淋巴结肿大(LNs)。PET-CT显示右乳腺肿块18F-FDG活性增加,隔膜两侧的LN,脾脏肿大,还有骨髓.右侧乳腺肿块活检显示TNBC。患者接受了R-CHOP的新辅助治疗,并获得了乳腺肿瘤的部分缓解。然而,TNBC在R-CHOP三个周期后进展。根据对乳腺肿块的下一代测序(NGS)分析,同源重组修复(HRR)缺陷(HRD)评分为72,新辅助方案改为利妥昔单抗加nab-紫杉醇和顺铂(R-TP),并导致明显的肿瘤消退。然后,患者接受了右乳房切除术,并进行了腋窝LN解剖。手术后,对患者进行定期监测,并给予R-TP和放疗辅助治疗.
    FL和HRD阳性TNBC的共存带来了诊断和治疗的挑战。基于多学科团队(MDT)讨论和NGS的有充分依据的新辅助策略在这种情况下保证了良好的结果。
    UNASSIGNED: Co-occurrence of breast cancer and non-Hodgkin\'s lymphoma is a rare condition with diagnostic and therapeutic challenges. The coexistence of follicular lymphoma (FL) and triple-negative breast cancer (TNBC) has not been described previously.
    UNASSIGNED: A 46-year-old woman, already suffering a history of untreated, advanced-stage, high tumor burden FL, was admitted for a rapidly progressing right breast mass. Ultrasonography showed an 8.3 × 3.6 × 4.1 cm fungating mass in the right breast with enlarged lymph nodes (LNs) in bilateral axillae. PET-CT demonstrated increased 18F- FDG activity in right breast mass, LNs on both sides of the diaphragm, enlarged spleen, and bone marrow. Biopsy of the right breast mass revealed TNBC. The patient underwent neoadjuvant therapy with R-CHOP and achieved partial response of breast tumor. However, TNBC progressed after three cycles of R-CHOP. According to the next-generation sequencing (NGS) assay on breast mass showing a homologous recombination repair (HRR) deficiency (HRD) score of 72, the neoadjuvant regimen was changed to rituximab plus nab-paclitaxel and cisplatin (R-TP) and resulted in significant tumor regression. The patient then underwent right mastectomy with an axillary LN dissection. After the surgery, she was regularly monitored and given adjuvant therapy with R-TP and radiotherapy.
    UNASSIGNED: The coexistence of FL and HRD-positive TNBC poses diagnostic and treatment challenges. Well-founded neoadjuvant strategy based on multidisciplinary team (MDT) discussion and NGS warranted a good outcome in this case.
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  • 文章类型: Case Reports
    通过临床影像学研究为甲状腺滤泡癌的治疗提供参考方法,1例甲状腺滤泡癌伴骨转移的病理特征和多模式治疗。
    通过识别病例的临床,成像,甲状腺滤泡癌骨转移的病理特征,反思病例的诊断和治疗过程,并参考有关甲状腺滤泡癌特征的文献,旨在为该类疾病的治疗提供参考。
    一名67岁男性患者入院,临床症状为左侧盆腔疼痛。活检病理显示高分化甲状腺组织。考虑到他的病史,结论甲状腺滤泡性癌可发生转移。在包括131I和局部和靶向药物的治疗组合之后,患者是稳定的并且没有观察到肿瘤进展。
    甲状腺滤泡癌易发生骨转移,骨转移是某些病例的首发症状。正确诊断需要临床影像学和病理学,成功的治疗需要多种方法的组合,包括131I,这是一种放射性碘疗法(RAI),局部治疗和靶向药物治疗。
    UNASSIGNED: To provide reference method for the treatment of thyroid follicular carcinoma by studing the clinical imaging, pathological features and multimodal treatment of a case of thyroid follicular carcinoma with bone metastasis.
    UNASSIGNED: By identifying the case\'s clinical, imaging, pathological features of a case of thyroid follicular carcinoma with bone metastasis, reflecting on the case\'s diagnosis and treatment process, and referring to literature about the characteristics of thyroid follicular carcinoma, the study aims to provide reference for the treatment of this kind of disease.
    UNASSIGNED: A 67-year-old male patient was admitted to the hospital with clinical symptoms of left pelvic pain. The biopsy pathology showed well-differentiated thyroid tissue. Considering his medical history, conclusion of thyroid follicular carcinoma metastasis could be made.The patient was stable and no tumor progression was observed after a combination of therapies including 131I and topical and targeted agents.
    UNASSIGNED: Thyroid follicular carcinoma are prone to bone metastasis, and bone metastasis is the first symptom in some cases. Clinical imaging and pathology are needed for correct diagnosis, and a successful treatment requires a combination of multiple approaches including 131I, which is a Radioactive Iodine Therapy(RAI), local therapy and targeted drug therapy.
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  • 文章类型: Journal Article
    UNASSIGNED:多学科团队(MDT)方法长期以来一直被认为是为乳腺癌患者提供高标准护理的最佳方法。随着越来越多的患者和越来越复杂的病例,MDT对时间和资源的压力越来越明显。因此,当地医院部门必须调整其MDT流程,以更好地简化讨论并优化效率。巴斯的皇家联合医院是英国的地区综合医院。每年大约有500名癌症患者接受治疗,MDT每周讨论约60名患者。
    UNASSIGNED:为了改进我们的MDT会议流程并提高生产率,我们使用MicrosoftAccess™创建了一个简洁的MDT模板:让所有临床医生能够实时添加患者和信息。我们还分配了每周准备时间,因此高级临床医生确保所有患者在会议之前做好准备,并在可能的情况下预先填充结果和潜在结果。
    UNASSIGNED:我们记录了在实施改变前后6次MDT会议期间讨论患者的时间。病例按病理类别分类以确定制剂变化后是否存在差异。总的来说,我们显著缩短了我们的平均MDT讨论时间(p=0.02).我们显着减少了术后恶性病例(p<0.0006)和预期良性核心活检病例(p<0.0047)的平均讨论时间,允许适当地重新分配时间来讨论更复杂的案件,讨论复杂放射学病例的时间显着增加(p<0.025)。
    UNASSIGNED:我们提供了一种有效的方法来改善MDT会议的准备和演示,方法是确保每位患者在会议前做好适当的准备。这些简单案例的结果已经预先填充。这在会议中创造了额外的时间来讨论更复杂的临床病例,同时允许团队的所有成员在需要时讨论所有患者。
    UNASSIGNED: The multidisciplinary team (MDT) approach has long been considered the optimal way in which to deliver a high standard of care to patients with breast cancer. With a growing number of patients and ever-increasing complexity of cases, the strain on time and resource of the MDT is becoming increasingly evident. It is therefore essential that local hospital departments adapt their MDT processes to better streamline discussions and optimise efficiency. The Royal United Hospital in Bath is a district general hospital in the UK. Approximately 500 patients with cancers are treated annually, and the MDT discusses approximately 60 patients per week.
    UNASSIGNED: To improve our MDT meeting processes and increase productivity, we created a concise MDT template using Microsoft Access™: giving all clinicians the ability to add patients and information in real time. We also allocated weekly preparation time whereby a senior clinician ensured all patients were prepared prior to the meeting with results and potential outcomes prepopulated where possible.
    UNASSIGNED: We recorded the time spent discussing patients during 6 MDT meetings before and after implementation of changes. Cases were classified by pathology category to determine if there were differences following the preparation changes. Overall, we significantly reduced our average MDT discussion time (p=0.02). We significantly reduced average discussion time in postoperative malignant cases (p<0.0006) and expected benign core biopsy cases (p<0.0047), allowing appropriate redistribution of time towards discussion of more complex cases, reflected by the significant increase in time spent discussing complex radiology cases (p<0.025).
    UNASSIGNED: We offer an effective method for improving the MDT meeting preparation and presentation by ensuring each patient is appropriately prepared prior to the meeting, and outcomes for those simple cases are already prepopulated. This creates additional time within the meeting to discuss more complex clinical cases while allowing all members of the team an opportunity to discuss all patients if needed.
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  • 文章类型: Journal Article
    麻风病是由麻风分枝杆菌(M.leprae),并且在疾病的慢性性及其长期治疗方案方面是独特的。即使在世界卫生组织(WHO)引入多种药物治疗(MDT)之后,每年报告大量麻风病新病例(近20万例),指示主动传输,尤其是在发展中国家。MDT后复发的临床表现可由于麻风病反应而发生,复发或再感染。很难区分反应,复发和再感染。在这里,我们通过根据证据将其与反应和复发区分开来并通过分析患者的临床数据,将最近一例麻风病复发病例归类为再感染。
    Leprosy is caused by Mycobacterium leprae (M. leprae) and is unique in terms of the chronicity of the disease and its prolonged treatment protocol. Even after the introduction of multidrug therapy (MDT) by World health organization (WHO), large numbers of new cases (nearly 200,000) of leprosy are reported yearly, indicating active transmission, especially in developing countries. Recurrent clinical manifestations after MDT can occur due to leprosy reactions, relapse or reinfection. It is very difficult to differentiate reaction, relapse and reinfection. Here we categorized a recent case of reoccurrence of leprosy as reinfection by differentiating it from reaction and relapse based on evidence and by analysing the clinical data of the patient.
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  • 文章类型: Case Reports
    背景:深盆腔子宫内膜异位症(DPE)引起的子宫外子宫内膜间质肉瘤(EESS)生活质量差,术前难以诊断。然而,患者的生活质量可以提高,当它被准确地诊断和管理成功。
    方法:一名35岁女性患者就诊于我院,有3个月的便血和肛门疼痛病史。最初,她被误诊为直肠间质瘤,然后在几次多学科小组(MDT)会议后,被准确诊断为患有DPE的EESS.通过促性腺激素释放激素激动剂(GnRH-α)治疗使病变缩小,然后以最小的创伤切除。
    结论:MDT对患者的治疗至关重要。可促进个体化治疗,提高患者的生活质量。
    Extrauterine endometrial stromal sarcoma (EESS) arising from Deep pelvic endometriosis (DPE) has a poor life quality and is difficult to diagnose pre-operatively. However, the patient\'s quality of life can be improved when it is diagnosed precisely and managed successfully.
    A 35-year-old woman presented to our hospital with a 3-month history of hematochezia and anal pain. Initially, she was misdiagnosed as a rectal stromal tumor and then precisely diagnosed as having EESS from DPE following several multidisciplinary team (MDT) meetings. The lesion was shrunk by gonadotrophin-releasing hormone agonist (GnRH-α) treatment and then resected with minimal trauma.
    MDT is crucial in the treatment of the patient. It can promote individualized treatment and improve patient\'s quality of life.
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  • 文章类型: Case Reports
    Objectives: Tinnitus is the perception of sound without any external auditory stimulus. Cervicogenic somatic tinnitus (CST) is a subset in which symptoms are modulated by maneuvers of the neck. The evidence for effective diagnosis and treatment of CST is limited. Mechanical Diagnosis and Therapy (MDT) is a biopsychosocial assessment and management system that uses the response to mechanical forces to classify clinical presentations accurately. The purpose of this case report is to describe the MDT assessment and management of a patient with chronic subjective tinnitus.Methods: A 67-year-old female with a 5-year history of left-sided subjective tinnitus, neck pain, and headache was referred for physiotherapy. Outcome measures included the Visual Analogue Scale (VAS), Tinnitus Handicap Inventory (THI), and Neck Disability Index (NDI). She was evaluated and treated according to MDT principles with management consisting of individualized directional preference exercises and postural correction.Results: Significant improvements in symptoms, cervical range of motion, function, and psychosocial status were observed over the long-term. At 6 months, THI scores dropped from 62/100 to 18/100 and NDI scores dropped from 18/50 to 3/50.Discussion: A comprehensive MDT assessment led to a classification of Derangement, with treatment focusing on tailored self-management. Contrary to other interventions described for CST, the patient was able to make significant and lasting changes to her symptoms without the need for any externally applied interventions. The emphasis on self-management dovetails well with the biopsychosocial model of care. This case provides preliminary evidence for the utility of screening for Derangement in conservative tinnitus assessments.Level of Evidence: 4.
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  • 文章类型: Case Reports
    目的:Morton神经瘤(MN)是一种累及跖骨区足底指神经的神经痛。MN的循证治疗方案很少,物理治疗(PT)的效用未知。机械诊断和治疗(MDT)是一种分类系统,基于对重复的末端运动的机械和症状反应,利用针对骨科疾病的方向特定治疗。本案例系列的目的是描述使用MDT分类系统对三名患有MN医学诊断的患者的管理。方法:三名年龄在54-75岁之间的单侧足底前足疼痛持续6周至8年的女性患者,在临床公认的MN诊断标准阳性后,由足病医生转诊,包括放射学影像学和激发试验。使用MDT评估和治疗原则对患者进行评估和治疗。干预包括与患者腰椎(1例)或远端肢体(2例)的方向偏好相匹配的重复运动。结果:立即和一年的结果是极好的,显示快速和持久的改善。放电后,患者无症状或能够自我管理,而无需寻求额外的医疗干预。每位患者的总就诊频率平均为8-16天的2-3次就诊。讨论:对重复的末端运动测试的反应允许对运动进行分类和处方,以快速改善三名接受PT服务并经医学诊断为MN的患者的症状和功能。该系列提供了初步证据,证明MDT可以有效地对MN患者进行分类和治疗。
    Objectives: Morton\'s neuroma (MN) is a neuralgia involving the common plantar digital nerves of the metatarsal region. Evidence-based treatment options for MN are sparse, and utility of physical therapy (PT) is unknown. Mechanical Diagnosis and Therapy (MDT) is a classification system utilizing direction-specific treatment for orthopedic conditions based on mechanical and symptomatic response to repeated end range movements. The purpose of this case series is to describe the management of three patients with a medical diagnosis of MN using the MDT classification system.Methods: Three female patients aged 54-75 years with unilateral plantar forefoot pain for 6 weeks to 8 years were referred by a podiatrist following positive clinically accepted diagnostic criteria for MN including radiological imaging and provocation testing. Patients were evaluated and treated utilizing MDT assessment and treatment principles. The intervention consisted of repeated movements matched to the patient\'s directional preference at either the lumbar spine (1 patient) or distal extremity (2 patients).Results: Immediate and one-year outcomes were excellent, demonstrating rapid and lasting improvement. Following discharge, the patients have been asymptomatic or able to self-manage without seeking additional medical intervention for this condition. Total visit frequency per patient averaged 2-3 visits total across 8-16 days.Discussion: Responses to repeated end range movements testing allowed for classification and prescription of exercise to rapidly improve symptoms and function in three patients referred to PT services with medically diagnosed MN. This series provides preliminary evidence that MDT may be effective in classifying and treating patients with MN.
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  • 文章类型: Journal Article
    The patient in this case study presented with constant idiopathic neck pain and left lower scapular pain (greater than 3 months) and was treated based on the principles of Mechanical Diagnosis and Therapy (MDT). Retraction exercises produced centralization of the lower scapular pain to the upper part of the scapula at the initial visit. At the first visit, the performance level on the Cranio-Cervical Flexion Test (CCFT) was ≤20 mmHg before the treatment. At the conclusion of the treatment during which centralization occurred, the CCFT level improved to 24 mmHg. At the second visit, all symptoms were abolished and cervical range of motion (ROM) was fully restored by performing repeated extension in lying from a retracted position with clinician\'s traction. The CCFT levels before and immediately after the treatment were 24 and 26 mmHg, respectively. At the third visit (1 week after the initial visit), he noted that all daily activities could be performed without pain. The CCFT level was maintained at 26mmHg. The patient in this study showed immediate improvement in the CCFT through the treatments based on MDT. This suggests a possible link between MDT interventions and motor control of the cervical spine and a need to further investigate this relationship.
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