Yilmaz Sabri, Kozakewich Harry P, Alomari Ahmad I, Fishman Steven J, Mulliken John B, Chaudry Gulraiz
Vascular Anomalies Center, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.
Pediatr Radiol. 2014 May;44(5):558-65. doi: 10.1007/s00247-014-2876-5. Epub 2014 Feb 2.
Infantile hemangiomas demonstrate a pattern of proliferative growth in infancy followed by a slow phase of involution. In contrast a rare type of vascular tumor, intramuscular capillary-type hemangioma, usually presents beyond the period of infancy with nonspecific symptoms and no evidence of involution.
The purpose of this study was to characterize the clinical, imaging, histopathological characteristics and management of intramuscular capillary-type hemangioma.
We performed a retrospective review of a 20-year period to identify children diagnosed with intramuscular capillary-type hemangioma. Patient demographics, imaging and histopathological findings were recorded.
We included 18 children (10 boys, 8 girls) with histologically proven intramuscular capillary-type hemangioma - and adequate imaging. The mean age at presentation was 8.1 years (range 1 day to 19 years). Twelve lesions involved muscles of the extremities, 4 were located in the trunk and 2 were in the head and neck. MRI had been performed in all children and demonstrated a soft-tissue mass with flow voids, consistent with fast flow. The lesion was well-circumscribed in 16 children and intralesional fat was seen in 14. Doppler US demonstrated a heterogeneous lesion, predominantly isoechoic to surrounding muscle, with enlarged arterial feeders. Enlarged feeding arteries, inhomogeneous blush and lack of arteriovenous shunting were noted on angiography (n = 5). The most common histopathological findings were lobules of capillaries with plump endothelium and at least some adipose tissue. The lesions were excised in six children. Two children were lost to follow-up. In the remaining 10, follow-up MRI studies ranging from 3 months to 10 years showed that the lesion enlarged in proportion to the child (n = 7), demonstrated slow growth (n = 2) or remained stable (n = 1). There was no change in imaging characteristics on follow-up.
Intramuscular capillary-type hemangioma is a rare benign vascular tumor of skeletal muscle. The most typical imaging features show a heterogeneous intramuscular mass with fast flow, and intralesional fat. Although the lesion is relatively stable in appearance over time, imaging does not obviate the need for a biopsy to rule out sarcoma. The diagnosis can usually be established by typical findings on histopathology.
婴儿血管瘤在婴儿期呈现增殖性生长模式,随后进入缓慢的消退期。相比之下,一种罕见的血管肿瘤,即肌内毛细血管型血管瘤,通常在婴儿期之后出现,症状不具有特异性,且无消退迹象。
本研究旨在描述肌内毛细血管型血管瘤的临床、影像学、组织病理学特征及治疗方法。
我们对20年期间诊断为肌内毛细血管型血管瘤的儿童进行了回顾性研究。记录了患者的人口统计学资料、影像学和组织病理学检查结果。
我们纳入了18例经组织学证实为肌内毛细血管型血管瘤且有充分影像学资料的儿童(10例男孩,8例女孩)。就诊时的平均年龄为8.1岁(范围1天至19岁)。12个病变累及四肢肌肉,4个位于躯干,2个位于头颈部。所有儿童均进行了MRI检查,显示为有血流空洞的软组织肿块,提示血流速度快。16例儿童的病变边界清晰,14例可见瘤内脂肪。多普勒超声显示病变不均匀,主要与周围肌肉等回声,有增粗的供血动脉。血管造影(n = 5)显示供血动脉增粗、造影剂充盈不均匀且无动静脉分流。最常见的组织病理学表现为内皮细胞饱满的毛细血管小叶和至少一些脂肪组织。6例儿童的病变进行了切除。2例儿童失访。其余10例中,随访MRI检查时间为3个月至10年,结果显示病变与儿童生长成比例增大(n = 7),生长缓慢(n = 2)或保持稳定(n = 1)。随访期间影像学特征无变化。
肌内毛细血管型血管瘤是一种罕见的骨骼肌良性血管肿瘤。最典型的影像学特征是不均匀的肌内肿块,血流速度快,且有瘤内脂肪。尽管随着时间推移病变外观相对稳定,但影像学检查不能排除活检以排除肉瘤的必要性。通常通过组织病理学的典型表现即可确诊。