Dey Ashish, Ahuja Anmol, Mittal Tarun, Sheikh Mohd Taha Mustafa, Dhawan Shashi, Malik Vinod K
Department of General and Laparoscopic Surgery, Sir Ganga Ram Hospital, New Delhi, India.
Department of Pathology, Sir Ganga Ram Hospital, New Delhi, India.
J Minim Access Surg. 2022 Jan-Mar;18(1):136-138. doi: 10.4103/jmas.JMAS_317_20.
Proliferative fasciitis (PF) is a rare pseudosarcomatous lesion arising from the subcutaneous fascia and the fibrous septa. Only few hundred cases have been reported in the literature. In the largest series of 53 patients, only two patients had PF lesion arising from the flank. The most common site of origin is extremities followed by abdomen and head and neck. Its origin from the abdominal wall layer and presentation as the fever has been rarely reported in the literature. A PF lesion larger than 5 cm dimension has been sparsely noted. We report the presence of this rare entity in a 68-year-old gentleman who presented to us with low-grade fever and the presence of large lump arising from the abdominal wall. In our patient, the lesion was arising from transervsalis fascia and was excised in toto laparoscopically without damaging the abdominal muscles. It is imperative to differentiate both these lesions from sarcoma on histopathological examination as the follow-up treatment protocols for both vary.
增殖性筋膜炎(PF)是一种罕见的假肉瘤性病变,起源于皮下筋膜和纤维间隔。文献中仅报道了数百例。在最大的一组53例患者中,只有2例PF病变起源于侧腹。最常见的起源部位是四肢,其次是腹部以及头颈部。其起源于腹壁层并表现为发热的情况在文献中鲜有报道。尺寸大于5厘米的PF病变也很少被提及。我们报告了一名68岁男性患者存在这种罕见疾病,该患者因低热以及腹壁出现大肿块前来就诊。在我们的患者中,病变起源于腹横筋膜,通过腹腔镜完整切除,未损伤腹部肌肉。在组织病理学检查中,必须将这两种病变与肉瘤区分开来,因为两者的后续治疗方案不同。