TY - JOUR
T1 - Spontaneous regression of multiple intracranial capillary hemangiomas in a newborn—long-term follow-up and literature review
AU - Noureldine, Mohammad Hassan A.
AU - Rasras, Saleh
AU - Safari, Hosein
AU - Sabahi, Mohammadmahdi
AU - Jallo, George I.
AU - Arjipour, Mahdi
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.
PY - 2021/10
Y1 - 2021/10
N2 - Background: Intracranial capillary hemangiomas (ICHs) have a natural history and behavior that is very different from intracranial cavernous malformations. The literature is not consistent as to the best management strategy for ICHs. Case description: Our patient is a 40-day-old male infant who presented with progressive increase in head circumference and multiple cutaneous capillary and ICHs. Obstructive hydrocephalus necessitated urgent cerebrospinal fluid (CSF) diversion, but no other surgical intervention was pursued due to the high risk-to-benefit ratio. All intracranial lesions spontaneously regressed by 11 years of age, albeit at a slower speed than the cutaneous lesions, with no functional or cognitive sequelae. We conducted a comprehensive literature review and provided a summary of all reported ICH cases. Conclusion: Asymptomatic patients with ICHs are best approached with close follow-up and serial imaging studies as the potential for spontaneous regression is relatively high. Patients with isolated lesions or unclear diagnoses may benefit from a stereotactic biopsy, and surgical resection should be reserved for symptomatic lesions only.
AB - Background: Intracranial capillary hemangiomas (ICHs) have a natural history and behavior that is very different from intracranial cavernous malformations. The literature is not consistent as to the best management strategy for ICHs. Case description: Our patient is a 40-day-old male infant who presented with progressive increase in head circumference and multiple cutaneous capillary and ICHs. Obstructive hydrocephalus necessitated urgent cerebrospinal fluid (CSF) diversion, but no other surgical intervention was pursued due to the high risk-to-benefit ratio. All intracranial lesions spontaneously regressed by 11 years of age, albeit at a slower speed than the cutaneous lesions, with no functional or cognitive sequelae. We conducted a comprehensive literature review and provided a summary of all reported ICH cases. Conclusion: Asymptomatic patients with ICHs are best approached with close follow-up and serial imaging studies as the potential for spontaneous regression is relatively high. Patients with isolated lesions or unclear diagnoses may benefit from a stereotactic biopsy, and surgical resection should be reserved for symptomatic lesions only.
KW - Capillary hemangioma
KW - Infantile hemangioma
KW - Intracranial
KW - Spontaneous regression
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U2 - 10.1007/s00381-021-05053-7
DO - 10.1007/s00381-021-05053-7
M3 - Article
C2 - 33481102
AN - SCOPUS:85099739051
SN - 0256-7040
VL - 37
SP - 3225
EP - 3234
JO - Child's Nervous System
JF - Child's Nervous System
IS - 10
ER -