Dolan G, Smith J, Reilly J T
Department of Haematology, Northern General Hospital, Sheffield, UK.
Postgrad Med J. 1991 Oct;67(792):914-5. doi: 10.1136/pgmj.67.792.914.
We report the case of a 55 year old man who presented as Pancoast's syndrome associated with a left sided Horner's syndrome, a mass in the left supraclavicular fossa and marked weakness with wasting of the left arm consistent with a left sided brachial plexus lesion. Biopsy revealed the typical features of lymphomatoid granulomatosis. Neurological involvement is a rare presenting manifestation of this uncommon disease. Lymphomatoid granulomatosis should be considered as a rare but potentially treatable cause of Pancoast's syndrome.
我们报告了一例55岁男性患者，该患者表现为潘科斯特综合征，伴有左侧霍纳综合征、左锁骨上窝肿块以及与左侧臂丛神经病变相符的左臂明显无力和萎缩。活检显示为淋巴瘤样肉芽肿的典型特征。神经系统受累是这种罕见疾病罕见的首发表现。淋巴瘤样肉芽肿应被视为潘科斯特综合征的一种罕见但可能可治疗的病因。
