Mondor disease

Mondor 病
  • 文章类型: Case Reports
    Mondor病是主要位于胸腹壁的浅表性血栓性静脉炎,中上臂,和阴茎。这种疾病可以影响所有30岁以上的人,无论种族,种族,但对女性的影响大于男性。本研究案例的重要性在于成为阿尔巴尼亚首例报告的Mondor病病例。
    方法:在本研究中,据报道,一例浅表血栓性静脉炎影响右胸壁的胸腹静脉。注意到乳房下外象限有明显的脐带。病人,一名49岁的女性从2021年3月开始绝经,出现胸痛,应该进行两个月的夸大体力活动。
    进行了详细的主观和客观检查。所有实验室数据,包括COVID-19检测,显示除ESR外的正常范围值。布洛芬治疗2周,胸痛消退,但胸壁可触及的脊髓持续存在。
    结论:回顾文献并在彩色多普勒检查后得出此诊断结论。由于以前没有这种临床病例的经验,因此很难确定诊断。
    UNASSIGNED: Mondor Disease is superficial thrombophlebitis mostly located in the thoracic-abdominal wall, mid-upper arm, and penis. The disease can affect all people over 30 years old regardless of race, ethnicity but affects women more than men. The importance of this study case consists on being the first reported case of Mondor Disease in Albania.
    METHODS: In this study, a case of superficial thrombophlebitis affecting the thoraco-epigastric veins in the right chest wall is reported. Evidence of a palpable cord in the inferior outer quadrant of the breast was noted. The patient, a 49-year-old female who has been in menopause from March of 2021, presented with chest pain ought to two months of exaggerated physical activity.
    UNASSIGNED: A detailed subjective and objective examination was performed. All laboratory data, including tests for COVID-19, showed normal range value except ESR. For 2 weeks under treatment with Ibuprofen, the chest pain was subsided but the palpable cord in the chest wall was persistent.
    CONCLUSIONS: Reviewing the literature and after the Color Doppler examination it has been concluded in this diagnose. It was difficult to determine the diagnosis because of no previous experience with such clinical case.
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  • 文章类型: Case Reports
    阴茎Mondor病是一种罕见的疾病,其特征是阴茎背侧浅静脉血栓形成,其发病机制尚不清楚。长期或积极的性交已被确定为潜在的危险因素。我们介绍了一例54岁的男子,他在侵略性活动后出现了阴茎肿块。对背浅静脉血栓的诊断采用超声诊断,MRI证实。患者接受保守治疗并放弃性活动。四周后,观察到血栓完全消退.这个案例强调了医疗保健专业人员的重要性,尤其是泌尿科医生,在识别和管理阴茎蒙多的疾病。
    Penile Mondor\'s disease is a rare condition characterized by superficial dorsal vein thrombosis of the penis, whose pathogenesis remains unclear. Prolonged or aggressive sexual intercourse has been identified as a potential risk factor. We present a case of a 54-year-old man who developed a penile mass following aggressive sexual activity. Diagnosis of superficial dorsal vein thrombosis was made using ultrasound and confirmed by MRI. The patient underwent conservative treatment and abstained from sexual activity. After four weeks, complete resolution of the thrombus was observed. This case emphasizes the importance of healthcare professionals, particularly urologists, in recognizing and managing Penile Mondor\'s disease.
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  • 文章类型: Case Reports
    阴茎蒙多病(MD)是一种明显的,痛苦,阴茎背侧浅静脉血栓形成引起的皮下硬结。我们报告了一例阴茎MD,怀疑与长期口服西地那非有关。一名46岁的男子在性交后7小时出现持续的阴茎疼痛和肿胀,来到了我们的急诊科。他间歇性地使用口服西地那非11年,并在服用西地那非后的前一天晚上进行性交。检查未发现生殖器区域与性交有关的创伤或阴茎皮肤温度升高的证据。然而,注意到阴茎背部静脉突出的阴茎肿胀和压痛。立即进行彩色多普勒超声检查,显示右侧阴茎背侧浅静脉扩张的高回声血栓形成,软组织肿胀,血栓性病变中没有可检测到的血流信号。患者被诊断为患有阴茎MD。患者接受保守治疗。一些报道表明西地那非参与血栓形成。医生应该意识到,长期口服西地那非可能与阴茎MD有关。
    Penile Mondor disease (MD) is a palpable, painful, subcutaneous induration caused by superficial dorsal penile vein thrombosis. We report a case of penile MD that was suspected to be related to prolonged oral sildenafil use. A 46-year-old man visited our emergency department with sustained penile pain and swelling that began 7 hours after sexual intercourse. He had used oral sildenafil intermittently for 11 years and engaged in sexual intercourse the previous night after taking sildenafil. Examination revealed no evidence of intercourse-related trauma to the genital area or an increase in penile skin temperature. However, penile swelling and tenderness over the protruding dorsal penile vein were noted. A color Doppler ultrasound examination was performed immediately, which showed hyperechoic thrombosis in the right superficial dorsal penile vein that was dilated, with soft tissue swelling and no detectable flow signal in the thrombotic lesion. The patient was diagnosed as having penile MD. The patient was treated conservatively. Some reports have indicated the involvement of sildenafil in thrombogenesis. Physicians should be aware that prolonged oral sildenafil use may be associated with penile MD.
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  • 文章类型: Case Reports
    背景:先天性耻骨前窦是在下腹部中线发现的罕见异常。新生儿先天性耻骨前窦通常无症状,并且诊断通常是在从耻骨区域的先前存在的孔中自发挤出脓性物质之后的以后生活中实现的。我们介绍了一例先天性耻骨前窦包皮环切术后出现脓性分泌物的病例。一个4岁的高加索男孩出现在我们的泌尿科门诊诊所,他的阴茎背侧远端有脓性分泌物。他有在另一个中心进行包皮环切术的历史,6个月前.他的父母说,尽管使用了各种抗生素,脓性分泌物持续了6个月,孩子在包皮环切术前没有任何抱怨。据报道他的情况是浅背静脉血栓形成,被称为阴茎蒙多病,在以前的医院进行的磁共振成像。体格检查显示,他的阴茎远端有一个小的针孔病变,一个刚性的圆柱形管延伸到阴茎的近侧。我们通过小型血管导管注射对比剂进行了血管造影,并确认了耻骨前窦的诊断。进行了手术探查和长鼻窦,显然在他的耻骨联合前表面以纤维束结束,被发现并切除。
    结论:先天性耻骨前窦手术前,排除阴茎Mondor病和包皮环切术并发症(尤其是感染性并发症)的可能性是非常重要的,这类似于先天性耻骨前窦.
    BACKGROUND: Congenital prepubic sinus is a rare anomaly found in the midline of the lower abdomen. Congenital prepubic sinus is usually asymptomatic in neonates, and a diagnosis is often achieved later in life after spontaneous extrusion of purulent material from the pre-existing hole in the pubic region. We present a case of congenital prepubic sinus presenting with purulent discharge after circumcision. A 4-year-old Caucasian boy presented to our urology out-patient clinic with purulent discharge from the distal part of the dorsum of his penis. He had a history of circumcision performed at a different center, 6 months ago. His parents stated that although various antibiotics were used, the purulent discharge continued for 6 months and the child had no complaints before circumcision. His condition was reported as superficial dorsal venous thrombosis, known as penile Mondor disease, in magnetic resonance imaging that was performed in the previous hospital. A physical examination revealed a small pinhole lesion at the distal part of his penis and a rigid cylindrical tube extending to the proximal side of his penis. We performed fistulography by injecting contrast material through a small angiocatheter and confirmed the diagnosis of prepubic sinus. Surgical exploration was performed and a long sinus, apparently ending as a fibrous tract at the anterior surface of his pubic symphysis, was found and resected.
    CONCLUSIONS: Before congenital prepubic sinus surgery, it is critically important to rule out penile Mondor disease and the possibility of a circumcision complication (especially infective complications) mimicking congenital prepubic sinus.
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