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Seborrheic keratoses: a distinctive diagnoses of pigmented vulvar lesions: a case report. 脂溢性角化病:色素外阴病变的独特诊断:1例报告。
Pub Date : 2010-02-10 DOI: 10.1186/1757-1626-3-56
Esra Aktepe Keskin, Canan Gorpelioglu, Evren Sarifakioglu, Hasan Kafali

Seborrheic keratoses, a benign growth lesion, is a very common cutaneous lesion encountered in white races in the fourth and fifth decade. The occurrence of this lesion on the vulva is rare, as an isolated lesion or in association with lesions elsewhere. A 34-year-old woman reported with a hyperpigmented palpable lesion, approximately 5-10 mm in diameter, was found on the patient's left labium majus. The clinical differential diagnosis of the pigmented lesions of the vulva is difficult often need a biopsy.

脂溢性角化病是一种良性生长病变,在白人中是一种非常常见的皮肤病变。这种病变在外阴的发生是罕见的,作为一个孤立的病变或与其他地方的病变相关联。一位34岁的女性报告了一个可触及的色素沉着病变,直径约5-10毫米,在患者的左唇。外阴色素性病变的临床鉴别诊断是困难的,往往需要活检。
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引用次数: 0
Healing enhancement of chronic venous stasis ulcers utilizing H-WAVE(R) device therapy: a case series. 利用H-WAVE(R)装置治疗促进慢性静脉淤积性溃疡的愈合:一个病例系列。
Pub Date : 2010-02-10 DOI: 10.1186/1757-1626-3-54
Kenneth Blum, Amanda Lh Chen, Thomas Jh Chen, B William Downs, Eric R Braverman, Mallory Kerner, Stella Savarimuthu, Anish Bajaj, Margaret Madigan, Seth H Blum, Gary Reinl, John Giordano, Nicholas Dinubile

Introduction: Approximately 15% (more than 2 million individuals, based on these estimates) of all people with diabetes will develop a lower-extremity ulcer during the course of the disease. Ultimately, between 14% and 20% of patients with lower-extremity diabetic ulcers will require amputation of the affected limb. Analysis of the 1995 Medicare claims revealed that lower-extremity ulcer care accounted for $1.45 billion in Medicare costs. Therapies that promote rapid and complete healing and reduce the need for expensive surgical procedures would impact these costs substantially. One such example is the electrotherapeutic modality utilizing the H-Wave(R) device therapy and program.It has been recently shown in acute animal experiments that the H-Wave(R) device stimulation induces a nitric oxide-dependent increase in microcirculation of the rat Cremaster skeletal muscle. Moreover, chronic H-wave(R) device stimulation of rat hind limbs not only increases blood flow but induces measured angiogenesis. Coupling these findings strongly suggests that H-Wave(R) device stimulation promotes rapid and complete healing without need of expensive surgical procedures.

Case presentation: We decided to do a preliminary evaluation of the H-Wave(R) device therapy and program in three seriously afflicted diabetic patients. Patient 1 had chronic venous stasis for 6 years. Patient 2 had chronic recurrent leg ulcerations. Patient 3 had a chronic venous stasis ulcer for 2 years. All were dispensed a home H-Wave(R) unit. Patient 1 had no other treatment, patient 2 had H-Wave(R) therapy along with traditional compressive therapy, and patient 3 had no other therapy.For patient 1, following treatment the ulcer completely healed with the H-Wave(R) device and program after 3 months. For patient 2, by one month complete ulcer closure occurred. Patient 3 had a completely healed ulcer after 9 months.

Conclusions: While most diabetic ulcers can be treated successfully on an outpatient basis, a significant proportion will persist and become infected. Based on this preliminary case series investigation we found that three patients prescribed H-Wave(R) home treatment demonstrate accelerated healing with excellent results. While these results are encouraging, additional large scale investigation is warranted before any interpretation is given to these interesting outcomes.

大约15%(超过200万人,基于这些估计)的糖尿病患者将在病程中发展为下肢溃疡。最终,14%到20%的下肢糖尿病溃疡患者将需要截肢。对1995年医疗保险索赔的分析显示,下肢溃疡的护理占医疗保险费用的14.5亿美元。促进快速和完全愈合并减少昂贵外科手术需求的治疗方法将大大影响这些费用。其中一个例子是利用H-Wave(R)装置治疗和程序的电疗方式。最近在急性动物实验中显示,H-Wave(R)装置刺激诱导大鼠Cremaster骨骼肌微循环一氧化氮依赖性增加。此外,慢性h波(R)装置刺激大鼠后肢不仅能增加血流量,还能诱导血管生成。结合这些发现强有力地表明,H-Wave(R)装置刺激促进快速和完全愈合,而不需要昂贵的外科手术。病例介绍:我们决定对3例严重糖尿病患者进行H-Wave(R)装置治疗和方案的初步评估。患者1慢性静脉淤积6年。患者2有慢性复发性腿部溃疡。患者3患有慢性静脉淤积性溃疡2年。每个人都被分配了一个家用H-Wave(R)装置。患者1未接受其他治疗,患者2在传统压缩治疗的基础上进行H-Wave(R)治疗,患者3未接受其他治疗。对于患者1,使用H-Wave(R)装置和程序治疗3个月后溃疡完全愈合。患者2,1个月溃疡完全愈合。患者3在9个月后溃疡完全愈合。结论:虽然大多数糖尿病溃疡可以在门诊成功治疗,但很大一部分会持续存在并发生感染。基于这一初步的病例系列调查,我们发现三名患者采用H-Wave(R)家庭治疗显示出加速愈合的良好效果。虽然这些结果令人鼓舞,但在对这些有趣的结果进行任何解释之前,还需要进行额外的大规模调查。
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引用次数: 6
Recurrent vitreous occlusion of glaucoma drainage device tube in a patient with glaucoma in aphakia: a case report. 无晶状体青光眼患者复发性青光眼引流管玻璃体闭塞1例。
Pub Date : 2010-02-10 DOI: 10.1186/1757-1626-3-55
Ghee Soon Ang, Yi Wei Goh, Augusto Azuara-Blanco

Patients with spontaneous lens dislocation and glaucoma can be challenging to manage. We present a forty-six year old Caucasian lady who was referred with bilateral high intraocular pressure, and was subsequently diagnosed with glaucoma in association with lens dislocation and Marfan syndrome. Baerveldt glaucoma drainage device tubes were inserted in both eyes due to poor response to medical therapy. However, this was complicated by recurrent vitreous occlusion of both glaucoma drainage tubes requiring further multiple surgical interventions. There have not been any further recurrences of vitreous incarceration or posterior segment complications since, but the patient remains under close follow-up.

自发性晶状体脱位和青光眼患者的治疗具有挑战性。我们报告一位46岁的白人女性,她因双侧高眼压而就诊,随后被诊断为青光眼并伴有晶状体脱位和马凡氏综合征。Baerveldt青光眼引流管因药物治疗效果不佳而被植入双眼。然而,这是复杂的反复玻璃体阻塞的两个青光眼引流管需要进一步的多次手术干预。此后没有再发生玻璃体嵌顿或后段并发症,但患者仍在密切随访中。
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引用次数: 0
Four different malignancies in one patient: a case report. 一个病人有四种不同的恶性肿瘤:一份病例报告。
Pub Date : 2010-02-08 DOI: 10.1186/1757-1626-3-53
Umut Demirci, Ugur Coşkun, Pinar Uyar Göçün, Bahar Gurlek, Burcu Saka, Banu Oztürk, Mustafa Benekli, Süleyman Büyükberber

Cancer survivors have a higher risk of new primary cancer, in the same or in another organ, than the general population. We report a 78-year-old women who has metachronous quadruple adenocarcinoma, includes bilateral breast cancer, ovarian cancer and retroperitoneal neuroendocrine carcinoma. The development of second cancer in cancer survivors can be expected but third or higher order malignancies are rare.

与一般人群相比,癌症幸存者在同一器官或其他器官中患新发原发性癌症的风险更高。我们报告一位78岁的女性患有异时性四重腺癌,包括双侧乳腺癌、卵巢癌和腹膜后神经内分泌癌。癌症幸存者中第二种癌症的发展是可以预期的,但第三种或更高级别的恶性肿瘤是罕见的。
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引用次数: 6
A case of pregnancy with Rhesus antibody and bicornuate uterus - a favourable outcome: a case report. 一例妊娠与恒河猴抗体和双角子宫-一个有利的结果:一个病例报告。
Pub Date : 2010-02-03 DOI: 10.1186/1757-1626-3-50
Santanu Acharya, Samia Ahmed

Introduction: In 1% of Rhesus negative women sensitisation occurs without any overt sensitising event during pregnancy. This accounts for late immunisation during a first pregnancy and is responsible for 18-27% of cases of alloimmunisation. The incidence of congenital uterine anomalies in a fertile population is 3.2% of which 5% are bicornuate uterus. Bicornuate uterus can lead to early miscarriages, preterm labor, fetal growth retardation and congenital malformations.

Case presentation: A 23-year-old lady in her first pregnancy developed Anti-D antibodies at 28 weeks of gestation without any known sensitising event. In view of increasing anti-D titres, at 36 weeks she was delivered. Incidentally during caesarean section she was found to have bicornuate uterus. The neonate was treated with phototherapy and blood transfusion following delivery.

Conclusion: Rhesus antibodies when managed by close monitoring and timely delivery can lead to favourable outcome. Bicornuate uterus does not always lead to complications like miscarriage, growth retardation or preterm labour and does not need any special intervention.

简介:1%的恒河阴性妇女在怀孕期间没有任何明显的致敏事件。这是首次怀孕期间的晚期免疫接种,占同种异体免疫接种病例的18-27%。在有生育能力的人群中,先天性子宫异常的发生率为3.2%,其中5%为双角子宫。双角子宫可导致早期流产、早产、胎儿发育迟缓和先天性畸形。病例介绍:一名23岁的首次怀孕的女性在妊娠28周时出现了抗d抗体,没有任何已知的致敏事件。鉴于抗d滴度增高,36周分娩。在剖腹产时,她被发现有双角子宫。新生儿在分娩后接受了光疗和输血治疗。结论:恒河猴抗体的密切监测和及时交付可导致良好的结果。双角子宫并不总是导致流产、发育迟缓或早产等并发症,也不需要任何特殊干预。
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引用次数: 3
Subcutaneus leiomyosarcoma of the neck: a case report. 颈部皮下平滑肌肉瘤1例。
Pub Date : 2010-02-03 DOI: 10.1186/1757-1626-3-52
Charalampos Skoulakis, Theognosia S Chimona, Paraskevi Tsirevelou, Chariton E Papadakis

Introduction: Leiomyosarcomas are rare tumors. The most common site for head and neck leiomyosarcomas is the oral cavity, followed by sinonasal tract and skin. Subcutaneous leiomyosarcomas are thought to arise from small to medium-sized blood vessels in the subcutaneous tissue.

Case presentation: A 67-year-old female patient underwent excision of a slow growing neck mass of the left posterior neck triangle after a thorough clinical and laboratory examination. The lesion was located in the subcutis and fine needle aspiration biopsy revealed malignant features. Histology revealed subcutaneous leiomyosarcoma and the patient is free from local recurrence and distant metastases 3 years after wide excision of the lesion.

Conclusions: The primary modality of therapy of subcutaneous leiomyosarcoma is surgery, adjuvant radiotherapy or chemotherapy may be used for control of local recurrence, in case of positive surgical margins, high-grade or large tumors.

平滑肌肉瘤是一种罕见的肿瘤。头颈部平滑肌肉瘤最常见的部位是口腔,其次是鼻道和皮肤。皮下平滑肌肉瘤被认为起源于皮下组织的中小血管。病例介绍:一位67岁的女性患者在经过彻底的临床和实验室检查后,接受了左侧后颈部三角缓慢生长的颈部肿块切除术。病变位于皮下,细针穿刺活检显示恶性特征。组织学显示为皮下平滑肌肉瘤,患者在广泛切除病变3年后无局部复发和远处转移。结论:皮下平滑肌肉瘤的治疗方式以手术为主,手术切缘阳性、肿瘤高级别或较大时,可采用辅助放疗或化疗控制局部复发。
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引用次数: 13
Severe odynophagia in a patient developing after azithromycin intake: a case report. 阿奇霉素摄入后患者出现严重厌食:1例报告。
Pub Date : 2010-02-03 DOI: 10.1186/1757-1626-3-48
Umit Akyuz, Yusuf Erzin, Fevzi Firat Yalniz, Ibrahim Volkan Senkal, Isin Dogan Ekici, Cengiz Pata

Introduction: Drug-induced esophageal ulcers most commonly cause heartburn, midsternal pain and dysphagia. In our clinic azithromycin is a relative widely used antibiotic for respiratory tract infections and otitis media because of its activity against Haemophilus influenzae and atypical pathogens, and its ease of administration. After a thorough search in Pubmed the present case is the first one to report azithromycin-induced esophageal ulcer and associated symptoms in the literature.

Case presentation: A 61-year-old Caucasian man was admitted to our endoscopy unit for the investigation of odynophagia and retrosternal pain of new onset. His past medical history was unremarkable but had used azithromycin 500 mg/d for three days in the previous week. An upper endoscopy revealed an extensive serpiginous midesophageal ulcer in the presence of a normal squamocolumnar junction and biopsies from the edges and center of the lesion disclosed no neoplasia or infectious causes but a dense acute inflammatory infiltrate. The patient was put on a liquid diet, sucralfate proton pump inhibitor treatment and was symptom-free within two weeks. After four weeks on therapy a repeated upper endoscopic control examination demonstrated normal findings.

Conclusion: To our knowledge this is the first such a case of azithromycin -induced esophageal ulceration. We think that a little time taken by the physician to warn the patients for taking every oral drug with sufficient amount of water might prevent this kind of complications.

药物性食管溃疡最常引起胃灼热、胸骨中段疼痛和吞咽困难。在我们的临床中,阿奇霉素是一种相对广泛使用的抗生素,用于呼吸道感染和中耳炎,因为它对流感嗜血杆菌和非典型病原体有活性,而且易于给药。在Pubmed上彻底搜索后,本病例是文献中第一个报道阿奇霉素引起的食管溃疡及其相关症状的病例。病例介绍:一名61岁的白人男性因新发的咽痛和胸骨后疼痛被内镜检查部门收治。既往病史无明显差异,但曾于前一周使用阿奇霉素500 mg/d,连续3天。上腔镜检查发现食管中部广泛的蛇形溃疡,伴有正常的鳞状柱连接处,病变边缘和中心活检未发现瘤变或感染性原因,但有密集的急性炎症浸润。患者给予液体饮食、硫硫铝质子泵抑制剂治疗,两周内症状消失。治疗四周后,反复上肢内窥镜控制检查显示正常。结论:据我们所知,这是首例阿奇霉素引起的食管溃疡。我们认为,如果医生花一点时间提醒患者服用每一种口服药物时都要喝足量的水,可能会防止这种并发症的发生。
{"title":"Severe odynophagia in a patient developing after azithromycin intake: a case report.","authors":"Umit Akyuz,&nbsp;Yusuf Erzin,&nbsp;Fevzi Firat Yalniz,&nbsp;Ibrahim Volkan Senkal,&nbsp;Isin Dogan Ekici,&nbsp;Cengiz Pata","doi":"10.1186/1757-1626-3-48","DOIUrl":"https://doi.org/10.1186/1757-1626-3-48","url":null,"abstract":"<p><strong>Introduction: </strong>Drug-induced esophageal ulcers most commonly cause heartburn, midsternal pain and dysphagia. In our clinic azithromycin is a relative widely used antibiotic for respiratory tract infections and otitis media because of its activity against Haemophilus influenzae and atypical pathogens, and its ease of administration. After a thorough search in Pubmed the present case is the first one to report azithromycin-induced esophageal ulcer and associated symptoms in the literature.</p><p><strong>Case presentation: </strong>A 61-year-old Caucasian man was admitted to our endoscopy unit for the investigation of odynophagia and retrosternal pain of new onset. His past medical history was unremarkable but had used azithromycin 500 mg/d for three days in the previous week. An upper endoscopy revealed an extensive serpiginous midesophageal ulcer in the presence of a normal squamocolumnar junction and biopsies from the edges and center of the lesion disclosed no neoplasia or infectious causes but a dense acute inflammatory infiltrate. The patient was put on a liquid diet, sucralfate proton pump inhibitor treatment and was symptom-free within two weeks. After four weeks on therapy a repeated upper endoscopic control examination demonstrated normal findings.</p><p><strong>Conclusion: </strong>To our knowledge this is the first such a case of azithromycin -induced esophageal ulceration. We think that a little time taken by the physician to warn the patients for taking every oral drug with sufficient amount of water might prevent this kind of complications.</p>","PeriodicalId":87572,"journal":{"name":"Cases journal","volume":"3 ","pages":"48"},"PeriodicalIF":0.0,"publicationDate":"2010-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1757-1626-3-48","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"28757257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Giant cell tumor of the anterior rib masquerading as a breast mass: a case report and review of current literature. 前肋骨巨细胞瘤伪装成乳房肿块:1例报告及文献回顾。
Pub Date : 2010-02-03 DOI: 10.1186/1757-1626-3-51
Nicole D Riddle, Hideko Yamauchi, Jamie T Caracciolo, David Cheong, Nazanin Khakpour, Marilyn M Bui

Introduction: Giant cell tumor (GCT) is an aggressive, but usually benign bone neoplasm most commonly arising in the metaphysis/epiphyses of long bones. While they are categorized as benign tumors, they can be locally aggressive and clinically have metastatic potential. The most common locations of this tumor include the distal femur, proximal tibia, and distal radius. We report a GCT arising in an atypical location and mimicking a breast mass.

Case presentation: This case was diagnosed at a large cancer center in Florida. Pertinent clinical findings were obtained from chart review and inter-departmental consultation. Radiologically, the initial impression included a deep-seated breast cancer with local chest wall invasion. Further evaluation revealed the mass to be an expansile rib lesion with extraosseous soft tissue invasion. Histological examination of the biopsy specimen showed bland multi-nucleated giant cells and mononuclear cells whose nuclei were morphologically similar. No necrosis, pleomorphism or mitotic activity was identified. No chondroid or osseous elements were present.

Conclusion: The histological features of bland mononuclear and multinucleated giant cells along with the lack of any additional mesenchymal elements led to the diagnosis of giant cell tumor. Resection of tumor was performed. The patient is disease free as of the last follow-up visit. This case is important as it shows where the physician must keep this diagnosis in mind whenever a deeply located breast mast is present.

巨细胞瘤(GCT)是一种侵袭性的,但通常是良性的骨肿瘤,最常见于长骨干骺端。虽然它们被归类为良性肿瘤,但它们可能是局部侵袭性的,临床上具有转移潜力。这种肿瘤最常见的位置包括股骨远端、胫骨近端和桡骨远端。我们报告一个GCT产生在一个不典型的位置和模仿乳房肿块。病例介绍:这个病例是在佛罗里达州的一个大型癌症中心诊断出来的。相关的临床结果通过图表回顾和跨部门会诊获得。影像学表现为深部乳腺癌伴局部胸壁浸润。进一步的评估显示,肿块是一个扩张的肋骨病变与骨外软组织侵犯。活检标本的组织学检查显示平淡的多核巨细胞和单核细胞,细胞核形态相似。未发现坏死、多形性或有丝分裂活性。未见软骨或骨性成分。结论:巨细胞瘤的组织学特征为淡色的单核和多核巨细胞,且缺乏任何额外的间质成分,可作为巨细胞瘤的诊断依据。手术切除肿瘤。截至最后一次随访,患者无疾病。这个病例很重要,因为它表明,无论何时出现深部乳腺肥大,医生都必须牢记这一诊断。
{"title":"Giant cell tumor of the anterior rib masquerading as a breast mass: a case report and review of current literature.","authors":"Nicole D Riddle,&nbsp;Hideko Yamauchi,&nbsp;Jamie T Caracciolo,&nbsp;David Cheong,&nbsp;Nazanin Khakpour,&nbsp;Marilyn M Bui","doi":"10.1186/1757-1626-3-51","DOIUrl":"https://doi.org/10.1186/1757-1626-3-51","url":null,"abstract":"<p><strong>Introduction: </strong>Giant cell tumor (GCT) is an aggressive, but usually benign bone neoplasm most commonly arising in the metaphysis/epiphyses of long bones. While they are categorized as benign tumors, they can be locally aggressive and clinically have metastatic potential. The most common locations of this tumor include the distal femur, proximal tibia, and distal radius. We report a GCT arising in an atypical location and mimicking a breast mass.</p><p><strong>Case presentation: </strong>This case was diagnosed at a large cancer center in Florida. Pertinent clinical findings were obtained from chart review and inter-departmental consultation. Radiologically, the initial impression included a deep-seated breast cancer with local chest wall invasion. Further evaluation revealed the mass to be an expansile rib lesion with extraosseous soft tissue invasion. Histological examination of the biopsy specimen showed bland multi-nucleated giant cells and mononuclear cells whose nuclei were morphologically similar. No necrosis, pleomorphism or mitotic activity was identified. No chondroid or osseous elements were present.</p><p><strong>Conclusion: </strong>The histological features of bland mononuclear and multinucleated giant cells along with the lack of any additional mesenchymal elements led to the diagnosis of giant cell tumor. Resection of tumor was performed. The patient is disease free as of the last follow-up visit. This case is important as it shows where the physician must keep this diagnosis in mind whenever a deeply located breast mast is present.</p>","PeriodicalId":87572,"journal":{"name":"Cases journal","volume":"3 ","pages":"51"},"PeriodicalIF":0.0,"publicationDate":"2010-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1757-1626-3-51","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"28755526","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
A male presenting with a primary mucinous bladder carcinoma: a case report. 男性原发性膀胱粘液性癌1例报告。
Pub Date : 2010-02-03 DOI: 10.1186/1757-1626-3-49
Konstantinos Sigalas, Stavros I Tyritzis, Eleni Trigka, Ioannis Katafigiotis, Nikolaos Kavantzas, Konstantinos G Stravodimos

Background: The primary mucinous adenocarcinoma of the bladder is an extremely rare urologic entity, which is found in less than 2% of all urinary bladder tumours and is often presented as metastatic.

Case presentation: A 69-year old male patient was diagnosed with a primary mucinous adenocarcinoma of the bladder after undergoing a transurethral resection of a bladder tumour and complete examination of the entire gastrointestinal tract to rule out other primary cites. Immunohistochemistry confirmed the nature of the tumour. The patient underwent a radical cystoprostatectomy with en block bilateral pelvic lymphadenectomy and urinary diversion with a Bricker ileostomy.

Conclusion: The primary adenocarcinoma creates a diagnostic dilemma, since it cannot be easily differentiated by the adenocarcinoma that originates from the colon and the prostate. We advocate the radical surgical management, after exclusion of any primary malignant sites related to the gastrointestinal tract. The immunohistochemistry has a leading role, assisting with the differential diagnosis.

背景:原发性膀胱粘液腺癌是一种极其罕见的泌尿系统肿瘤,在所有膀胱肿瘤中不到2%的发生率,通常表现为转移性。病例介绍:一名69岁男性患者在接受经尿道膀胱肿瘤切除术和完整的胃肠道检查以排除其他原发城市后,被诊断为原发性膀胱粘液腺癌。免疫组织化学证实了肿瘤的性质。患者接受了根治性膀胱前列腺切除术,双侧盆腔淋巴结切除术和布瑞克回肠造口尿路转移。结论:原发性腺癌造成了一个诊断困境,因为它不容易与起源于结肠和前列腺的腺癌区分。我们提倡根治性手术治疗,排除胃肠道相关的任何原发恶性部位后。免疫组织化学具有主导作用,有助于鉴别诊断。
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引用次数: 10
Depression, extrapyramidal symptoms, dementia and an unexpected outcome: a case report. 抑郁症、锥体外系症状、痴呆和意想不到的结果:一例报告。
Pub Date : 2010-02-02 DOI: 10.1186/1757-1626-3-47
Magda Tsolaki, Chaido Z Messini, Marianna Siapera, Foteini Fotiadou, Dionysia Delaporta, Athanasios Karatolias

Introduction: The diagnosis of Parkinson's disease is mainly clinical. DaT SCAN may help in difficult cases. Depression is also a clinical diagnosis and is common and persistent symptom in Parkinson's disease. Dementia is very often in Parkinson's disease, but usually not at the first stages. The treatment of each of the above symptoms is difficult and a lot of times individualized.

Case presentation: Female 64 years old patient with history of hypothyroidism, depression and anxiety disorder was examined at outpatient Memory and Dementia clinic of 3rd Department of Neurology. The patient's major problems were functional and cognitive decline, severe extrapyramidal symptoms and depression. According to UKPDS Brain Bank criteria the patient had bradykinesia, muscular rigidity, postural instability and rest tremor present with unilateral onset of the symptoms affecting left side most and progressive course. The modified Hoehn and Yahr scale was 3: mild to moderate bilateral disease; some postural instability; physically independent. The symptoms remained during nine months follow up, despite the pharmaceutical treatment. Nine months later, the patient made an attempt to suicide. Firstly, she was transferred to intensive care department with 2nd degree burns and respiratory problems, then she was hospitalized at the Burn Unit and afterwards at the Psychiatric clinic. One month later the patient had no depression, a clear reduction of the extrapyramidal symptoms, functional and cognitive improvement.

Conclusion: An astonishing improvement occurred after the threat of life. Two years after the attempt to suicide, the depressive symptoms remain in remission and functional and cognitive status is normal. The extrapyramidal symptoms have disappeared.

简介:帕金森病的诊断主要是临床诊断。DaT SCAN可以帮助在困难的情况下。抑郁也是帕金森病的一种临床诊断,是帕金森病常见且持续的症状。帕金森氏症中经常出现痴呆,但通常不是在最初阶段。以上每一种症状的治疗都很困难,而且很多时候都是个体化的。病例介绍:女性,64岁,有甲状腺功能减退、抑郁、焦虑病史,于神经内科第三科记忆与痴呆门诊就诊。患者的主要问题是功能和认知能力下降,严重的锥体外系症状和抑郁。根据UKPDS脑库标准,患者出现运动迟缓、肌肉僵硬、姿势不稳定和静止性震颤,症状以单侧发病的左侧为主,病程渐进。改进的Hoehn和Yahr评分为3:轻度至中度双侧疾病;一些体位不稳定;身体上的独立。在9个月的随访中,尽管进行了药物治疗,症状仍然存在。9个月后,病人企图自杀。首先,她因二度烧伤和呼吸问题被转到重症监护室,然后她住在烧伤科,后来住在精神科诊所。一个月后,患者没有抑郁,锥体外系症状明显减轻,功能和认知改善。结论:生命威胁后出现了惊人的改善。自杀未遂两年后,抑郁症状持续缓解,功能和认知状态正常。锥体外系症状消失了。
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引用次数: 4
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