Haghighi Kian Seyed Masoud, Jahanbakhshi Amin, Najafi Masoumeh, Ashtarinezhad Behnaz, Mokary Yousef, Zarimeidani Fatemeh
Department of Surgery, Surgery Research Center, School of Medicine, Rasool-E Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
Skull Base Research Center, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Int J Surg Case Rep. 2024 Jul;120:109896. doi: 10.1016/j.ijscr.2024.109896. Epub 2024 Jun 8.
Giant cell tumors of bone (GCTB) are infrequent tumors that usually impact the epiphyses of long bones and uncommonly manifest in the ribs. Herein, we report a case of asymptomatic GCTB directly invading the lung tissue.
A 36-year-old man was referred to our emergency department with only left chest pain. Computed tomography revealed a large heterogeneous solid cystic mass in the left lung apex and amorphous calcification and distraction in the posterior part of the left fourth rib. Histological examination also exhibited that the GCTB originated from the rib. The patient underwent an en-bloc resection with no recurrence in his one-year follow-up.
GCTB is characterized by osteoclast-like multinucleated giant cells and can exhibit aggressive local behavior. GCTB in the rib is rare, mainly found in the posterior arc. Radiographic features include lytic lesions with bone remodeling, often seen eccentrically in long bone epiphyses. Aggressive tumors may show cortical destruction and soft tissue extension. Surgery is often recommended for GCTB management, aiming for complete resection with sufficient surgical margins.
The absence of well-defined diagnostic criteria hinders the accurate diagnosis of GCTB, making a comprehensive assessment through radiological and histological examinations crucial. Upon physical examination, GCTB should be considered in the differential diagnosis for mediastinal lesions, regardless of their size. Furthermore, surgical removal can be taken into account as the primary treatment strategy for tumors that originate from the posterior arc of the ribs, such as GCTB.
骨巨细胞瘤(GCTB)是一种罕见肿瘤,通常累及长骨骨骺,很少在肋骨中表现。在此,我们报告一例无症状的GCTB直接侵犯肺组织的病例。
一名36岁男性因仅左侧胸痛被转诊至我院急诊科。计算机断层扫描显示左肺尖有一个大的异质性实性囊性肿块,左第四肋骨后部有不规则钙化和骨质破坏。组织学检查也显示GCTB起源于肋骨。患者接受了整块切除,在一年的随访中无复发。
GCTB的特征是破骨细胞样多核巨细胞,可表现出侵袭性局部行为。肋骨GCTB罕见,主要见于后肋弓。影像学特征包括伴有骨质重塑的溶骨性病变,常见于长骨骨骺的偏心部位。侵袭性肿瘤可能表现为皮质破坏和软组织侵犯。对于GCTB的治疗,通常建议手术,目标是在有足够手术切缘的情况下完整切除。
缺乏明确的诊断标准阻碍了GCTB的准确诊断,通过影像学和组织学检查进行综合评估至关重要。体格检查时,无论纵隔病变大小,鉴别诊断中均应考虑GCTB。此外,对于起源于肋骨后肋弓的肿瘤,如GCTB,可考虑手术切除作为主要治疗策略。