Burgener-Enderli Simone, Schmitt Andreas, Bassetti Stefano, Kirsch Mark
Division of Internal Medicine, University Hospital of Basel, Basel, Switzerland.
Division of Medical Oncology, University Hospital of Basel, Basel, Switzerland.
Eur J Case Rep Intern Med. 2025 Jul 3;12(8):005577. doi: 10.12890/2025_005577. eCollection 2025.
An 18-year-old woman presented to her general practitioner with a history of non-itching facial swelling, erythematous skin rash and a slightly coarse voice for a few days. She denied dyspnoea, B-symptoms and pain. Physical examination revealed generalized facial and neck swelling not involving the tongue or the oral mucous membranes. There was no lymphadenopathy. These findings resulted in the diagnosis of allergic angioedema and in oral treatment with corticosteroids and antihistamines. The swelling responded partially but reoccurred with dose reduction of the corticosteroids. Outpatient referrals to a dermatologist, an endocrinologist and a rheumatologist resulted in confirmation of the diagnosis of allergic angioedema, suspected iatrogenic Cushing syndrome and possible connective tissue disease, respectively. Three months after the first outpatient presentation the patient was admitted to our hospital with severe fatigue and left-sided chest pain. The clinical examination showed the known facial and neck swelling- and a sinus tachycardia (120 bpm) without any fever. Furthermore, the neck swelling seemed to be slightly asymmetrical. This was accompanied by leucocytosis, elevated C-reactive protein, and lactate dehydrogenase. An electrocardiogram showed sinus tachycardia (120/min) with a S1Q3-type. An ultrasound of the neck showed thrombosis of the left jugular vein. Subsequent computed tomography scan of the chest revealed a large mediastinal mass causing acute superior vena cava syndrome. Mediastinal large B-cell lymphoma was confirmed by biopsy. The patient underwent six cycles of DA-R-EPOCH (rituximab, etoposide, prednisolone, vincristine, cyclophosphamide, doxorubicin). Treatment resulted in complete response.
Vena cava superior syndrome is caused in over 60% of the cases by malignancies (bronchogenic carcinoma, lymphoma, germ cell tumour).Facial swelling, plethora of the upper chest without itchiness and hoarseness are classical symptoms of thoracic central venous obstruction.At every patient visit open-minded clinical reasoning should be used to avoid anchoring bias.
一名18岁女性因面部肿胀、无瘙痒的皮肤红斑和声音略粗就诊于全科医生,症状持续数天。她否认呼吸困难、B症状及疼痛。体格检查发现面部和颈部广泛性肿胀,但未累及舌头或口腔黏膜。无淋巴结肿大。这些表现诊断为过敏性血管性水肿,并给予口服皮质类固醇和抗组胺药治疗。肿胀部分消退,但在皮质类固醇减量时复发。门诊转诊至皮肤科医生、内分泌科医生和风湿科医生,分别确诊为过敏性血管性水肿、疑似医源性库欣综合征及可能的结缔组织病。首次门诊就诊3个月后,患者因严重疲劳和左侧胸痛入院。临床检查发现有已知的面部和颈部肿胀,窦性心动过速(120次/分),无发热。此外,颈部肿胀似乎略有不对称。伴有白细胞增多、C反应蛋白升高及乳酸脱氢酶升高。心电图显示窦性心动过速(120次/分),呈S1Q3型。颈部超声显示左侧颈静脉血栓形成。随后的胸部计算机断层扫描显示一个巨大纵隔肿块,导致急性上腔静脉综合征。经活检确诊为纵隔大B细胞淋巴瘤。患者接受了6个周期的DA-R-EPOCH(利妥昔单抗、依托泊苷、泼尼松龙、长春新碱、环磷酰胺、多柔比星)治疗。治疗后完全缓解。
超过60%的上腔静脉综合征病例由恶性肿瘤(支气管肺癌、淋巴瘤、生殖细胞瘤)引起。面部肿胀、上胸部充血且无瘙痒及声音嘶哑是胸段中心静脉阻塞的典型症状。每次患者就诊时都应采用开放的临床思维以避免锚定偏差。