A rare case of mesenchymal hamartoma of chest wall in a neonate

Harsha Sreedharan, Harveen Kaur, Rajsree Sreedevi, Joice Francis
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Abstract

Mesenchymal hamartoma of the chest wall (MHCW) is an extremely rare, benign lesion arising from one or more ribs. Typically, MHCW manifests as a unilateral lesion, yet there have been instances of multiple or bilateral occurrences documented. It is reported to have an increased male predisposition and the common presentation includes a visible chest wall mass. In asymptomatic neonates, conservative management is the preferred approach since there have been no reports of malignant transformation. Surgical intervention becomes necessary in cases where there is an active growth of the lesion or respiratory compromise. Here, we present a case of unilateral MHCW in a newborn being managed conservatively, followed by surgical resection at 2 months of age.
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一例罕见的新生儿胸壁间质火腿肠瘤病例
胸壁间质火腿肠瘤(MHCW)是一种极其罕见的良性病变,由一根或多根肋骨引起。胸壁间质肉芽肿通常表现为单侧病变,但也有多发或双侧病变的记录。据报道,该病的男性发病率较高,常见表现包括可见胸壁肿块。对于无症状的新生儿,保守治疗是首选方法,因为还没有恶性转化的报道。如果病变生长活跃或出现呼吸困难,则有必要进行手术治疗。在此,我们介绍一例单侧 MHCW 新生儿病例,该病例在保守治疗后于 2 个月大时进行了手术切除。
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