Ribigan Athena Cristina, Bajenaru Ovidiu Lucian, Antochi Florina Anca, Bajenaru Ovidiu Alexandru
University Emergency Hospital Bucharest, Neurology Department.
Ana Aslan National Institute of Geriatry and Geriatrics, Geriatry and Geriatrics Department.
Medicine (Baltimore). 2019 Jun;98(23):e15900. doi: 10.1097/MD.0000000000015900.
Hypertrophic osteoarthropathy, also named Pierre Marie-Bamberger syndrome, represents a rare medical condition that may be considered either a primary or a secondary disease, and lung malignancies are responsible for more than two-thirds of the cases with secondary forms of the disease.
We present the case of a 41-year-old man referred to our Neurology Department for pain that was considered secondary to cervical disc protrusions. The neurologic examination was normal. However, the general examination showed digital clubbing, right lateral cervical adenopathy, and pachydermia. The radiographic examinations of the upper and lower limbs depicted osseous abnormalities typical for periostosis, and the computed tomography of the thorax showed the presence of a mass lesion in the right upper pulmonary lobe. High values of vascular endothelial growth factor were also found. The patient was admitted to the Pneumology Clinic, where biopsy was performed from the lateral cervical adenopathy.
The anatomopathological examination revealed multiple neoplastic infiltrates suggestive of adenocarcinoma metastasis. Based on the clinical examination and radiological and histologic findings, the diagnosis of pulmonary adenocarcinoma with lymph nodes metastases and paraneoplastic hypertrophic osteoarthropathy was established.
The patient received treatment with nonsteroidal antiinflammatory drugs and opiate analgesics that relieved the pain.
The patient was referred to the Oncology Department for further treatment of the primary pathology. He received different types of chemotherapeutics, immunotherapy, and radiotherapy. However, despite all therapeutic measures, the disease rapidly progressed and the patient died 9 months later.
This is an interesting case of a patient with an overlooked pathology, which was refereed to our clinic for further investigations of a pain that was considered neuropathic, secondary to small cervical protrusions. Conversely, the pain proved to be nociceptive and Pierre Marie-Bamberger syndrome was the positive diagnosis in our patient, as it can be associated with numerous diseases, especially of neoplastic origin.
肥大性骨关节病,也称为皮埃尔·玛丽 - 班贝格综合征,是一种罕见的病症,可被视为原发性或继发性疾病,在继发性疾病形式中,超过三分之二的病例由肺部恶性肿瘤引起。
我们报告一例41岁男性患者,因被认为是颈椎间盘突出继发的疼痛转诊至我院神经科。神经系统检查正常。然而,全身检查发现杵状指、右侧颈部淋巴结肿大和皮肤增厚。上下肢的影像学检查显示了骨膜增生典型的骨质异常,胸部计算机断层扫描显示右上肺叶有一个肿块病变。还发现血管内皮生长因子值升高。患者被收入呼吸科门诊,对右侧颈部淋巴结进行了活检。
解剖病理学检查显示多处肿瘤浸润,提示腺癌转移。根据临床检查以及放射学和组织学检查结果,确诊为肺腺癌伴淋巴结转移和副肿瘤性肥大性骨关节病。
患者接受了非甾体类抗炎药和阿片类镇痛药治疗,疼痛得到缓解。
患者被转诊至肿瘤科进一步治疗原发性疾病。他接受了不同类型的化疗、免疫治疗和放疗。然而,尽管采取了所有治疗措施,疾病仍迅速进展,患者9个月后死亡。
这是一个有趣的病例,患者的病情被忽视,最初因被认为是由小的颈椎间盘突出继发的神经性疼痛转诊至我院进一步检查。相反,后来证明疼痛是伤害性的,皮埃尔·玛丽 - 班贝格综合征是我们患者的确诊病症,因为它可能与多种疾病相关,尤其是肿瘤起源的疾病。