Bergas Alba, Escrihuela-Vidal Francesc, Fernández Calvo Davinia, Capdevila Pons Olga, Corbella Xavier
Department of Internal Medicine, Hospital Universitari de Bellvitge, Bellvitge Biomedical Research Institute-IDIBELL, L'Hospitalet de Llobregat, Spain.
Department of Pathology, Hospital Universitari de Bellvitge, Bellvitge Biomedical Research Institute-IDIBELL, L'Hospitalet de Llobregat, Spain.
Eur J Case Rep Intern Med. 2020 Oct 29;7(12):001944. doi: 10.12890/2020_001944. eCollection 2020.
Spontaneous haemothorax (SH) is a rare subcategory of haemothorax that involves the accumulation of blood within the pleural space in the absence of trauma. SH especially occurs in middle-aged or elderly patients, but data are usually limited to case reports and case series. Coagulopathy, aneurysm or aortic dissection, Rendu-Osler-Weber syndrome and malignancy have to be considered among the causes of SH.
We describe a case of primary angiosarcoma of the spleen presenting as relapsing haemothorax.
An 81-year-old woman was referred to our hospital because of a 2-month history of relapsing haemothorax after the performance of urgent splenectomy due to active bleeding from large spleen cysts. No evidence of neoplasm was seen after pathological examination of the spleen. On admission, left haemothorax and 2 new cystic masses in the thoracic wall were documented, both in close relation to the scars of previous surgery and chest tubes. After excision of 1 mass, histological examination revealed angiosarcoma, and a final diagnosis of primary angiosarcoma of the spleen with postsurgical metastatic dissemination to the thorax and pleura was made.
Primary angiosarcoma should be included in the differential diagnosis of haemorrhagic spleen cysts. Clinical diagnosis and management usually requires splenectomy, but it should be carefully planned in order to avoid local metastatic dissemination or haematogenous spread of the tumour.
The differential diagnosis of spleen cysts must include malignant conditions.Despite its absolute rarity, angiosarcoma is considered the most common primary non-haematolymphoid splenic malignancy and has a poor prognosis.Splenectomy is usually required for a prompt diagnosis of primary angiosarcoma of the spleen, but it needs to be performed with extreme caution to avoid metastatic dissemination.
自发性血胸(SH)是血胸的一种罕见亚型,指在无创伤情况下胸膜腔内血液积聚。SH尤其多见于中年或老年患者,但数据通常仅限于病例报告和病例系列。凝血功能障碍、动脉瘤或主动脉夹层、遗传性出血性毛细血管扩张症和恶性肿瘤等都应被视为SH的病因。
我们描述一例以复发性血胸为表现的脾脏原发性血管肉瘤病例。
一名81岁女性因巨大脾囊肿活动性出血行急诊脾切除术后2个月出现复发性血胸被转诊至我院。脾脏病理检查未发现肿瘤证据。入院时,发现左侧血胸及胸壁有2个新的囊性肿物,均与既往手术及胸管瘢痕关系密切。切除其中1个肿物后,组织学检查显示为血管肉瘤,最终诊断为脾脏原发性血管肉瘤伴术后转移至胸部和胸膜。
原发性血管肉瘤应纳入出血性脾囊肿的鉴别诊断。临床诊断和治疗通常需要脾切除术,但应谨慎规划,以避免肿瘤局部转移或血行播散。
脾囊肿的鉴别诊断必须包括恶性情况。尽管血管肉瘤极为罕见,但被认为是最常见的原发性非血液淋巴系统脾脏恶性肿瘤,预后较差。通常需要进行脾切除术以迅速诊断脾脏原发性血管肉瘤,但必须极其谨慎地进行,以避免转移扩散。