Zeidan Bashar A, Abu Hilal Mohammed, Al-Gholmy Mohammed, El-Mahallawi Hanan, Pearce Neil W, Primrose John N
Hepato Pancreatico Biliary Surgery Unit - Southampton General Hospital, Southampton, SO16 6YD, UK.
World J Surg Oncol. 2006 Sep 20;4:66. doi: 10.1186/1477-7819-4-66.
Adenoid Cystic Carcinoma of the lacrimal gland is a rare tumour. Their aggressive behaviour, with a high-risk of local recurrence, and late distant spread of the tumour even after aggressive management has been reported. Metastasis to the liver is rare and when it occurs, it is usually part of widespread metastasis, and therefore surgical treatment is seldom considered.
We report a rare case of an isolated liver metastasis from a lacrimal gland adenoid cystic carcinoma 20 years after resection of the primary tumour. The patient presented with right upper quadrant pain radiating to the back and shortness of breath of 3 months duration. No local recurrence was detected during a 15 year follow-up with computerized tomography (CT) of the head. Abdominal CT scan demonstrated a solitary liver tumour with no other primary source, and the bone scan was normal. The patient was treated with an extended right hemihepatectomy. The histology revealed a predominantly cribriform tumour with focal areas of basaloid type metastatic lacrimal gland adenoid cystic carcinoma.
This case illustrates the unpredictable behaviour of adenoid cystic carcinoma and the need for a life long follow up for these patients after treatment. The possibility of surgical resection for liver metastasis from adenoid cystic carcinoma should always be considered.
泪腺腺样囊性癌是一种罕见的肿瘤。据报道,其具有侵袭性,局部复发风险高,即使经过积极治疗,肿瘤仍有晚期远处转移的情况。肝转移罕见,一旦发生,通常是广泛转移的一部分,因此很少考虑手术治疗。
我们报告一例罕见病例,患者在原发肿瘤切除20年后出现孤立性肝转移的泪腺腺样囊性癌。患者出现右上腹疼痛并放射至背部,伴有3个月的呼吸急促。在对头部进行15年的计算机断层扫描(CT)随访期间,未发现局部复发。腹部CT扫描显示有一个孤立的肝脏肿瘤,无其他原发灶,骨扫描正常。患者接受了扩大右半肝切除术。组织学检查显示主要为筛状肿瘤,伴有局灶性基底样型转移性泪腺腺样囊性癌。
本病例说明了腺样囊性癌的不可预测行为,以及这些患者治疗后需要终身随访。对于腺样囊性癌肝转移,应始终考虑手术切除的可能性。