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infantile hemangioma

Thursday 11 March 2004

juvenile hemangioma, cellular hemangioma of infancy, common hemangioma of infancy; GLUT1+ infantile hemangioma

Digital Cases (Digital slides)

- HPC/106 : GLUT1+ infantile hemangioma
- HPC:186 : GLUT1+ infantile hemangioma
- HPC:385 : GLUT1+ infantile hemangioma

Clinical synopsis

The typical infantile hemangioma appears postnataly, grows quickly, and regresses gradually in the first few years of life. Approximately one third of IH are present at birth.

Infantile hemangiomas progress through 3 stages: proliferative, involuting, and involuted. The proliferative phase is characterized by clinical growth. Once hemangiomas reach their maximum size, they begin to regress or involute. Histologically, this stage is characterized by endothelial apoptosis. Finally, the involuted stage of the hemangioma occurs when the original lesion is replaced by a connective tissue remnant. In contrast to hemangiomas, vascular malformations do not involute but continue to enlarge as the patient grows.

Morphological synopsis

These tumors are highly cellular, involving the dermis, often with extension into the subcutis. The tumor has a lobular architecture and plump endothelial cells. The latter cells express glut-1 antigens throughout the life of this tumor.

- lobular architecture

Developmental phases:

- proliferative phase
- involutive phase
- end-stage

Localization

- cutaneous infantile hemangioma
- extra-cutaneous GLUT1+ infantile hemangioma

Variants

- multiple infantile hemangioma (16880251)
- reticular infantile hemangioma (17845155)

Associations

- type 2 infantile hepatic hemangioendothelioma (16880251)

Differential diagnosis

- congenital hemangiomas

  • RICH (rapidly involuting congenital hemangioma)
  • NICH (non-involuting congenital hemangioma)

- vascular malformations

Immunochemsitry

- WT1+
- GLUT1+ (16230568)

Tumors GLUT1 WT1
infantile hemangioma + +
vascular malformation - -

Predisposition

- Beckwith-Wiedemann syndrome (15509684)
- familial predisposition at locus 5q31-33

Molecular biology

- monoclonality

β-Adrenergic receptor expression in vascular tumors (22743651)

Propranolol has recently emerged as an effective therapy for infantile hemangiomas causing regression.

The β-adrenergic receptor (AR) antagonist is thought to cause vasoconstriction by its effect on nitric oxide, block angiogenesis by its effect on vascular endothelial growth factor (VEGF), and induce apoptosis.

The expression of β2-AR (B2-AR) and its phosphorylated form (B2-ARP) have been identified in a case of infantile hemangioma that responded to propranolol treatment.

Although immunohistochemical expression of the receptors does not necessarily indicate that similar pathways of responsiveness to β-blockade are present, it does raises the possibility that β-blockade could potentially affect apoptosis and decrease responsiveness to VEGF.

See also

- vascular tumors
- vascular malformations (vascular dysplasia)
- cutaneous tumors

Reviews

- Vikkula M, Boon LM, Mulliken JB, Olsen BR. Molecular basis of vascular anomalies. Trends Cardiovasc Med. 1998 Oct;8(7):281-92. PMID: 14987552

References

- β-Adrenergic receptor expression in vascular tumors. Chisholm KM, Chang KW, Truong MT, Kwok S, West RB, Heerema-McKenney AE. Mod Pathol. 2012 Jun 29. PMID: 22743651

- Lawley LP, Cerimele F, Weiss SW, North P, Cohen C, Kozakewich HP, Mulliken JB, Arbiser JL. Expression of Wilms tumor 1 gene distinguishes vascular malformations from proliferative endothelial lesions. Arch Dermatol. 2005 Oct;141(10):1297-300. PMID: 16230568

- Timar J, Meszaros L, Orosz Z, Albini A, Raso E. WT1 expression in angiogenic tumours of the skin. Histopathology. 2005 Jul;47(1):67-73. PMID: 15982325

- Dadras SS, North PE, Bertoncini J, Mihm MC, Detmar M. Infantile hemangiomas are arrested in an early developmental vascular differentiation state. Mod Pathol. 2004 Sep;17(9):1068-79. PMID: 15143338

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