bleomycin

博来霉素
  • 文章类型: Case Reports
    博来霉素是一种具有出色抗肿瘤作用的糖肽抗生素。博来霉素的主要不良反应是肺纤维化。然而,白内障作为严重不良反应的发展尚未有报道。
    这里,我们描述了1例22岁男性睾丸癌患者通过博莱霉素治疗诱发白内障的病例.在手术干预和BEP方案的五个连续化疗周期后,包括博来霉素,依托泊苷和顺铂,患者报告视力逐渐无痛丧失,随着视觉能力的大幅下降,尤其是右眼。在全面的眼科检查之后,诊断为白内障。最终,患者接受了白内障超声乳化术和人工晶状体置换.
    博来霉素可引起白内障,这导致了视力的显著丧失。因此,临床医生应观察早期症状,适当调整治疗方法,防止症状加重。
    UNASSIGNED: Bleomycin is a glycopeptide antibiotic with outstanding anti-tumor effects. A major adverse effect of bleomycin is lung fibrosis. However, the development of cataracts as a severe adverse effect has not been reported.
    UNASSIGNED: Herein, we describe the first case of cataract induced by bleomycin therapy in a 22-year-old male with testicular cancer. After surgical intervention and following five successive chemotherapy cycles of the BEP regimen, including bleomycin, etoposide and cisplatin, the patient reported a gradual painless loss of vision, with substantial decline in visual ability, especially in the right eye. Following comprehensive eye examinations, a cataract was diagnosed. Eventually, the patient underwent phacoemulsification and received replacement of the intraocular lenses.
    UNASSIGNED: Bleomycin can cause cataracts, which induces a significant loss of vision. Therefore, clinicians should observe early symptoms and properly adjust treatment to prevent aggravation of symptoms.
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  • 文章类型: Journal Article
    背景:滋养细胞肿瘤通常与妊娠有关,非妊娠滋养细胞肿瘤极为罕见。非妊娠性卵巢绒毛膜癌(NGCO)是一种高度侵袭性的生殖细胞衍生肿瘤,经常表现为早期血行转移。
    方法:这里,我们报道一例28岁未婚女性月经规律,在末次月经周期后1周出现阴道出血.多普勒超声显示双侧附件肿块和血清人绒毛膜促性腺激素(hCG)水平升高。患者最初被误诊为异位妊娠。
    方法:最终病理证实国际妇产科联合会IANGCO期伴双侧卵巢成熟畸胎瘤。这是卵巢绒毛膜癌的一个非同寻常的例子,没有任何妊娠,而患者缺乏妊娠史,使得诊断被忽略。
    方法:初次手术和1周期博来霉素后,依托泊苷,顺铂(BEP)化疗,进行了腹腔镜保留生育功能的综合分期手术.术后给予两个周期的BEP化疗作为补充治疗,亮丙瑞林用于保护卵巢功能。
    结果:化疗结束后4个月月经恢复,肿瘤指标均在正常范围内。在36个月的随访中没有观察到复发的迹象。
    结论:如果女性患者出现不规则阴道出血和附件区域肿块,应考虑使用NGCO。本病例和我们的文献综述还强调,保留生育力的手术和多药化疗是治疗NGCO的有效方法。
    BACKGROUND: Trophoblastic neoplasms are often associated with pregnancy, and nongestational trophoblastic neoplasms are extremely rare. Nongestational ovarian choriocarcinoma (NGCO) is a highly aggressive germ cell-derived tumor frequently presenting with early hematogenous metastasis.
    METHODS: Herein, we report a case of a 28-year-old unmarried woman with regular menstruation who experienced vaginal bleeding 1 week after her last menstrual cycle. Doppler ultrasound revealed bilateral adnexal masses and elevated serum human chorionic gonadotropin (hCG) levels. The patient was initially misdiagnosed as presenting an ectopic pregnancy.
    METHODS: The final pathology confirmed an International Federation of Gynecology and Obstetrics stage IA NGCO with bilateral mature teratoma of the ovary. This is an extraordinary instance of ovarian choriocarcinoma which emerged without any prior gestation, and the patient\'s lack of a history of pregnancy made the diagnosis ignored.
    METHODS: After initial surgery and 1 cycle of bleomycin, etoposide, and cisplatin (BEP) chemotherapy, a laparoscopic fertility-preserving comprehensive staging surgery was performed. Two cycles of chemotherapy with BEP were administered as supplemental therapy postsurgery, and leuprorelin was administered to protect ovarian function.
    RESULTS: Menstruation resumed 4 months after chemotherapy completion, and tumor indicators were within the normal range. No signs of recurrence were observed at the 36-month follow-up.
    CONCLUSIONS: NGCO should be considered if a female patient exhibits irregular vaginal bleeding and masses in the adnexal area. The present case and our literature review also highlighted that fertility-sparing surgery and multidrug chemotherapy are effective methods for treating NGCO.
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  • 文章类型: Journal Article
    (1)背景:本病例系列和文献综述旨在评估电化学疗法在侵袭性脊柱血管瘤治疗中的疗效和安全性,呈现两个截然不同的案例。(2)方法:我们介绍了2例常规治疗难治性脊柱侵袭性血管瘤并接受了电化学治疗的病例。病例1涉及一名50岁的女性,她患有侵袭性L1脊髓血管瘤,此前曾接受过各种治疗,包括手术,放化疗,和动脉栓塞。病例2描述了一名16岁女性患有T12椎体血管瘤,以前接受过手术和稳定治疗,由于她的年龄和血管瘤的位置,她在治疗选择方面面临限制。(3)结果:在病例1中,在先前治疗失败后给予博来霉素的电化学疗法,并导致病灶大小的减小和临床症状的改善。在案例2中,由于与其他治疗相关的风险而选择了电化学疗法,并且在没有任何不良事件的情况下完成。两种情况都证明了电化学疗法作为脊柱血管瘤的可行治疗选择的潜力,尤其是在复杂或复发的病例中。(4)结论:当常规疗法不可行或失败时,博来霉素的电化学疗法是治疗侵袭性脊髓血管瘤的有希望的治疗方法。需要进一步的研究来建立明确的方案和脊柱血管瘤治疗中电化学疗法的长期结果。
    (1) Background: this case series and literature review aims to evaluate the efficacy and safety of electrochemotherapy in the management of aggressive spinal hemangiomas, presenting two distinct cases. (2) Methods: we present two cases of spinal aggressive hemangioma which were refractory to conventional treatments and underwent electrochemotherapy. Case 1 involves a 50-year-old female who presented with an aggressive spinal hemangioma of L1, who previously underwent various treatments including surgery, radio-chemotherapy, and arterial embolization. Case 2 describes a 16-year-old female with a T12 vertebral hemangioma, previously treated with surgery and stabilization, who faced limitations in treatment options due to her young age and the location of the hemangioma. (3) Results: in Case 1, electrochemotherapy with bleomycin was administered following the failure of previous treatments and resulted in the reduction of the lesion size and improvement in clinical symptoms. In Case 2, electrochemotherapy was chosen due to the risks associated with other treatments and was completed without any adverse events. Both cases demonstrated the potential of electrochemotherapy as a viable treatment option for spinal hemangiomas, especially in complex or recurrent cases. (4) Conclusions: electrochemotherapy with bleomycin is a promising treatment for aggressive spinal hemangiomas when conventional therapies are not feasible or have failed. Further research is needed to establish definitive protocols and long-term outcomes of electrochemotherapy in spinal hemangioma management.
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    文章类型: Case Reports
    背景:朗格汉斯细胞肉瘤(LCS)是一种非常罕见的朗格汉斯细胞恶性肿瘤,可能会转移到许多器官。该肿瘤诊断困难,预后差。
    目的:报告诊断LCS的困难,并讨论这种罕见实体的治疗管理。
    方法:我们报告一例52岁男性患者的LCS,表现为腋窝淋巴结肿大。结节性硬化型霍奇金病的诊断是在组织学检查后确定的。患者接受化疗(ABVD方案:阿霉素,博来霉素,长春碱,达卡巴嗪)和部分响应的放射治疗。然而,观察到疾病复发,组织学分析证实诊断为朗格汉斯细胞肉瘤。最初的组织学检查的修订从一开始就得出结论为肉瘤的诊断。我们选择了ESHAP(依托泊苷,甲基强的松龙,Aracytine,顺铂)方案和LCS的临床改善在2个周期后获得,但患者具有致命的结果并因疾病进展而死亡。
    结论:由于其稀有性,诊断困难,目前尚未确定该疾病的最佳治疗策略.多药化疗可能是治疗LCS的有效方式。
    BACKGROUND: Langerhans cell sarcoma (LCS) is a very rare malignant tumor of Langerhans cells that may metastasize to many organs. The diagnosis of this tumor is difficult and its prognosis is poor.
    OBJECTIVE: To report the difficulty to diagnose LCS, and discuss therapeutic management of this rare entity.
    METHODS: We report a case of LCS in a 52-year-old man who presented with an axillar lymphadenopathy. The diagnosis of nodular sclerosis type Hodgkin\'s disease was established after histologic examination. The patient was treated with chemotherapy (ABVD regimen: Doxorubicin, Bleomycin, Vinblastine, Dacarbazine) and radiotherapy with a partial response. However, disease recurrence was observed and histological analysis confirmed the diagnosis of Langerhans cell sarcoma. A revision of the initial histological examination concluded to the diagnosis of sarcoma from the beginning. We chose the ESHAP (Etoposide, Methylprednisolone, Aracytine, Cisplatin) regimen and clinical improvement of LCS was obtained after 2 cycles but the patient had a fatal outcome and died by disease progression.
    CONCLUSIONS: Because of its rarity, diagnosis is difficult and an optimal treatment strategy for this disease has not yet been identified. Polychemotherapy can be an effective modality for the treatment of LCS.
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  • 文章类型: Case Reports
    单个患者的多次外部宫颈根吸收(ECRR)病变的现象很少见,但可能与化学治疗剂博来霉素有关。该病例详述了一名成年男性,其在化疗后出现了多个ECRR病变。他对霍奇金淋巴瘤的治疗方案包括化疗抗生素博来霉素,以前与多个ECRR病变的发展有关。患者在同种异体干细胞移植后发生了移植物抗宿主病,这可能在ECRR病变的发展和促进中起重要作用。总的来说,八颗牙齿出现ECRR,检查时排除了所有已知的致病因素。据我们所知,这只是文献中第二例将博来霉素与多个ECRR病变联系起来的病例。本病例报告旨在使读者注意多个宫颈吸收病变可同时发展的事实。这些病变可能难以诊断和治疗,并且经常被误诊为龋齿。最后,读者应考虑博来霉素和移植物抗宿主病在ECRR多病变发展中的可能作用。
    The phenomenon of multiple external cervical root resorption (ECRR) lesions in a single patient is rare but may have a link with the chemotherapeutic agent bleomycin. This case details an adult male with multiple ECRR lesions that developed following chemotherapy. His treatment regimen for Hodgkin\'s lymphoma included the chemotherapeutic antibiotic bleomycin, which has previously been linked with development of multiple ECRR lesions. The patient developed graft versus host disease following an allogeneic stem cell transplant, which could have a significant role in the development and promotion of the ECRR lesions. In total, 8 teeth developed ECRR, and all the known causative factors were excluded when examined. To our knowledge, this is only the second reported case in the literature to link bleomycin to multiple ECRR lesions. This case report aims to bring the reader\'s attention to the fact that multiple cervical resorption lesions can develop simultaneously. These lesions can be difficult to diagnose and treat and are often misdiagnosed as caries. Finally, the reader should consider the possible role of bleomycin and graft versus host disease in development of multiple lesions of ECRR.
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  • 文章类型: Case Reports
    Kapososiform血管内皮瘤(KHE)是一种罕见的侵袭性血管肿瘤,主要发生在儿童中,在成人中很少见。我们报告了一例在成年患者眼睑上发现的KHE病例。
    我们介绍了一名成年患者,KHE在肿瘤切除后6个月复发。他接受了第二次手术切除和术中化疗。在3年的随访中没有复发的证据。
    成人KHE容易误诊。KHE可以通过手术切除来治疗。完全切除肿瘤和术中化疗可能有助于防止复发。
    UNASSIGNED: Kaposiform hemangioendothelioma (KHE) is a rare and invasive vascular tumor that mainly occurs in children and is rarely seen in adults. We report a case of KHE found on the eyelid of an adult patient.
    UNASSIGNED: We present an adult patient in whom KHE recurred 6 months after tumor resection. He underwent second surgical resection and intraoperative chemotherapy. There was no evidence of recurrence at the 3-year follow-up.
    UNASSIGNED: KHE in adults is easy to be misdiagnosed. KHE can be treated by surgical resection. Complete resection of the tumor and intraoperative chemotherapy may help prevent a recurrence.
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  • 文章类型: Case Reports
    背景:Brooke-Spiegler综合征是一种罕见的常染色体显性疾病,其特征是多发性良性皮肤附件肿瘤的持续发展。通常通过重复的标准手术来治疗。这里,我们提供了一项病例研究,其中使用电化学疗法(ECT)联合博来霉素作为治疗Brooke-Spiegler综合征患者晚期头颈部真皮圆柱瘤的有效替代方法.
    方法:一名45岁女性患者头皮上出现多发性复发性真皮圆柱瘤病变。先前的治疗包括几次手术切除,由于形成了许多疤痕和广泛的切除区域,导致心理恶化。提供ECT以提供肿瘤切除和疾病控制,并改善患者的生活质量。
    结果:治疗耐受性良好,肿瘤组织显著减少。重要的是,头皮皮肤状况明显改善,恢复边缘的卵泡密度。
    结论:该报告表明,博来霉素ECT作为一种侵入性较小的替代选择用于控制多个头皮圆柱瘤病变的可行性,具有美容上可接受的结果,提高生活质量。
    BACKGROUND: Brooke-Spiegler syndrome is a rare autosomal dominant disorder characterized by the continuous development of multiple benign skin appendage tumors. It is treated usually by repeated standard surgery. Here, we present a case study where electrochemotherapy (ECT) with bleomycin was used as an effective alternative approach in treating advanced dermal cylindromatosis of the head and neck in a patient with Brooke-Spiegler syndrome.
    METHODS: A 45-year-old woman presented with multiple recurrent dermal cylindroma lesions on her scalp. Previous treatment consisted of several surgical excisions that resulted in psychological deterioration due to the formation of numerous scars and extensive alopecic areas. ECT was offered to provide tumor removal and disease control and to improve the patient\'s quality of life.
    RESULTS: The treatment was well tolerated, and a significant reduction in neoplastic tissue was achieved. Importantly, scalp skin condition significantly improved, regaining a fair follicular density on the margins.
    CONCLUSIONS: This report suggests the feasibility of bleomycin ECT as a less invasive alternative option for controlling multiple scalp cylindroma lesions with cosmetically acceptable results, and improving quality of life.
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    文章类型: Review
    目的:探讨性腺外生殖细胞肿瘤的临床诊断和治疗方法。
    方法:分析在东部战区总医院诊治的1例性腺外生殖细胞肿瘤的临床资料,并复习相关文献。
    结果:患者最初被诊断为腹膜后肿瘤,由于肿瘤体积较大,通过切除肿瘤和左肾进行治疗,并发胰腺损伤。术后病理显示为性腺外生殖细胞恶性肿瘤。术后检查发现左侧睾丸占位,血清甲胎蛋白(AFP),人绒毛膜促性腺激素(hCG)和乳酸脱氢酶(LDH)阴性,然后进行第二阶段左睾丸切除,病理显示为睾丸精原细胞瘤。患者接受了7个疗程的顺铂,依托泊苷博莱霉素(PEB)方案,随访8年,没有发现复发或转移,患者在术后随访期间没有孩子。
    结论:对于有隐睾病史和位于中轴的肿瘤的患者,应特别注意睾丸的体检,睾丸超声检查,并测定AFP等指标以鉴别性腺肿瘤转移。如果是这样,可以首先考虑放疗和化疗,以减少手术并发症并实现准确管理。
    OBJECTIVE: To discuss the clinical diagnosis and treatment of extragonadal germ cell tumor.
    METHODS: We analyzed the clinical data on a case of extragonadal germ cell tumor diagnosed and treated in the General Hospital of Eastern Theater Command and reviewed the relevant literature.
    RESULTS: The patient was initially diagnosed with retroperitoneal tumor and treated by resection of the tumor together with the left kidney due to the large volume of the tumor, which was complicated by pancreatic injury. Postoperative pathology showed it to be extragonadal germ cell malignancy. Postoperative examination revealed space-occupying lesion in the left testis, with serum alpha fetoprotein (AFP), human chorionicgonadotropin (hCG) and lactate dehydrogenase (LDH) negative, followed by stage-two resection of the left testis, which was pathologically shown with testicular seminoma. The patient received 7 courses of cisplatin, etoposide bleomycin (PEB) regimen and was followed up for 8 years, which found no recurrence or metastasis, and the patient fathered no child during the postoperative follow-up.
    CONCLUSIONS: For patients with a history of cryptorchidism and tumors located in the central axis, special attention should be paid to physical examination of the testes, testicular ultrasonography, and determination of AFP and other indicators to identify gonadal tumor metastasis. And if so, radiotherapy and chemotherapy can be considered first to reduce surgical complications and achieve accurate management.
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  • 文章类型: Case Reports
    一名23岁的男性意识到左髋关节周围的疼痛,并参观了附近的骨科诊所。指出了右睾丸肿胀,怀疑是睾丸肿瘤.他被转诊到当地医院的泌尿科。血液分析显示甲胎蛋白(AFP)增加(3,620ng/ml)。计算机断层扫描(CT)扫描显示左髂骨骨转移和病态骨折。行根治性腹股沟睾丸切除术。病理检查发现混合生殖细胞肿瘤(胚胎癌和未成熟畸胎瘤:70%,精原细胞瘤:30%)。诊断为非精原细胞生殖细胞肿瘤,IIIc阶段,国际生殖细胞共识分类风险低。经过一个周期的博来霉素,依托泊苷和顺铂(BEP)方案,他被转诊到我们医院。经过总共4次BEP循环后,AFP正常化。Denosumab也每月给药。CT扫描显示骨转移减少,骨化恢复。骨活检未显示活的肿瘤细胞。因为切除剩余的肿块需要切除骨盆骨的左侧部分,左侧肢体功能明显丧失,我们在另外2个疗程的依托泊苷和顺铂方案后进行了密切随访.在最后一次全身化疗后45个月,患者目前还活着,没有复发。
    A 23-year-old male was aware of pain around his left hip joint and visited a nearby orthopedic clinic. Swelling of the right testis was pointed out, and a testicular tumor was suspected. He was referred to the urology department of a local hospital. Blood analysis showed an increase of α-fetoprotein (AFP) (3,620 ng/ml). Computed tomographic (CT) -scan revealed a left iliac bone metastasis and morbid fracture. Right radical inguinal orchiectomy was performed. The pathological examination revealed mixed germ cell tumor (embryonic carcinoma and immature teratoma: 70%, seminoma: 30%). The diagnosis was non-seminomatous germ cell tumor, stage IIIc, and poor risk on the International Germ Cell Consensus Classification. After one cycle of a bleomycin, etoposide and cisplatinum (BEP) regimen, he was referred to our hospital. After a total of 4 cycles of BEP, AFP was normalized. Denosumab was also administered monthly. The CT-scan showed a reduction of bone metastasis and recovery of ossification. Bone biopsy did not show viable tumor cells. Because extirpation of the remaining mass would require resection of the left part of the pelvic bone with significant functional loss of the left limb, we performed close follow-up after an additional 2 courses of the etoposide and cisplatin regimen. The patient is currently alive without recurrence at 45 months after the last systemic chemotherapy.
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  • 文章类型: Case Reports
    用博莱霉素硬化治疗可引起美容并发症,包括鞭毛状皮炎和色素沉着过度,由皮肤的微创伤引起或加剧。我们报告了一例9岁的小儿先天性血管畸形患者,其中使用了粘性绷带(例如,3MCoban)用于预防博来霉素诱导的色素沉着过度。术后和随访,我们的患者没有色素沉着过度或皮炎的迹象.本报告重点介绍了在博来霉素硬化治疗期间使用皮肤保护措施以改善术后预后。如果病人正在接受博莱霉素硬化治疗,考虑尽可能去除粘合剂,并使用粘性绷带固定线条,气道器械,和监控设备。
    Sclerotherapy with bleomycin can cause cosmetic complications, including flagellate dermatitis and hyperpigmentation, induced or exacerbated by microtrauma to the skin. We report a case of a 9-year-old pediatric patient with congenital vascular malformations in which a cohesive bandage (eg, 3M Coban) was utilized to prevent bleomycin-induced hyperpigmentation. Postoperatively and on follow-up, there were no signs of hyperpigmentation or dermatitis in our patient. This report highlights using skin protective measures during bleomycin sclerotherapy for improved postoperative outcomes. If a patient is undergoing bleomycin sclerotherapy, consider removing adhesive where possible and using cohesive bandage to secure lines, airway instruments, and monitoring equipment.
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