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Revista de Cirurgia e Traumatologia Buco-maxilo-facial

versão On-line ISSN 1808-5210

Rev. cir. traumatol. buco-maxilo-fac. vol.10 no.3 Camaragibe Jul./Set. 2010

 

ARTIGOS ORIGINAIS

 

Hemangiomas in newborns: an epidemiological study

 

Hemangiomas em recém-nascidos - estudo epidemiológico

 

 

Édila Figuerêdo FeitosaI; Fabiane Ferraz LimaII; Ana Paula Veras SobralIII

IOral Pathology Post-graduate. University of Pernambuco, Camaragibe, PE, Brazil
IIDentistry. University of Pernambuco, Camaragibe, PE, Brazil
IIIProfessor Oral Pathology. Oral Medicine Department. University of Pernambuco, Camaragibe, PE, Brazil

Corresponding author

 

 


ABSTRACT

OBJECTIVE: To identify the prevalence of hemangiomas in children born at Amaury de Medeiros Integrated Health Center between 1998 and 2008 and evaluate the characteristics of the children with this malformation.
STUDY DESIGN: The identification of hemangiomas by examining the record cards of the newly-born at the maternity hospital, noting the location of the lesion(s), child's gender and weight, prematurity, Apgar score and any additional malformations.
RESULTS: 68 children with hemangioma were identified, of whom 38 were girls. Regarding weight at birth, 58 of the newborns displayed adequate weight, 08 low weight, 1 very low weight and 1 extremely low weight. Two babies were born pre-term and sixty-six were born at term. The mean Apgar score was 8 with 62/91.2% of the babies presenting a normal Apgar score, 5/7.3% slight asphyxia and 1/1.5% moderate asphyxia. As to location, 61/89.7% presented hemangioma in the head and neck region and 6/8.8% in other parts of the body. The location was not recorded for 1 child.
CONCLUSIONS: Female babies were the most affected. Children who develop this malformation may have been born at term with a normal Apgar score and adequate weight. Most of the newborns showed isolated lesions on the head and neck. Complementary examinations should be requested as soon as a hemangioma is identified, since cell proliferation may affect the newborn's deep organs.

Keywords: Hemangioma, Hemangiomatosis, Sturge-Weber Syndrome, Vascular Malformation.


RESUMO

OBJETIVO: Identificar a prevalência de hemangiomas em crianças nascidas no Centro Integrado de Saúde Amaury de Medeiros entre os anos de 1998 e 2008, bem como observar as características das crianças que apresentam essa malformação.
DESENHO DO ESTUDO: Identificar hemangiomas através da análise dos prontuários de recém-nascidos da maternidade, bem como sua localização, gênero da criança, peso ao nascimento, APGAR e outras malformações associadas.
RESULTADOS: 68 recém-nascidos foram identificados; 38 meninas. Considerando o peso ao nascimento, 58 crianças apresentaram peso adequado, 08 crianças baixo peso, 01 peso muito baixo e 01 peso extremamente baixo. Sessenta e seis bebês nasceram a termo, frente a dois que nasceram prematuros. O escore médio do APGAR foi de 8 com 62/91.2% dos bebês exibindo APGAR normal, 05/7.3% exibindo asfixia leve, 01/1.5% asfixia moderada. Nenhuma criança exibiu asfixia grave. Em relação à localização, 61/89.7% dos recém-nascidos apresentavam hemangiomas na região de cabeça e pescoço, 06/8.8% exibiram hemangiomas em outras partes do corpo. Em 01 recém-nascido a localização do hemangioma não foi registrada.
CONCLUSÕES: O gênero feminino mostrou-se mais afetado por hemangiomas. Crianças que desenvolvem essa malformação podem nascer a termo, exibindo APGAR normal e com peso adequado. A maioria dos recém-nascidos apresentou lesões isoladas e em região de cabeça e pescoço. Exames complementares devem ser solicitados no momento em que forem identificados hemangiomas visíveis para se detectar possíveis lesões de acometimento em órgãos internos.

Palavras-chave: Hemangioma, Hemangiomatose, Síndrome de Sturge-Weber, Malformações Vasculares.


 

 

INTRODUCTION

Hemangiomas are the most common nonmalignant vascular tumors of infants, characterized by rapid endothelial cell proliferation and hypercellularity1,2. This condition may appear at birth and show rapid growth during the first infancy3,4,5. Some authors say the causes of the condition are unknown6,7; others report that 10% of cases has to do with family history8,9.

Actually, hemangiomas are classified as cutaneous (surface) or subcutaneous (deep) lesions. Hemangiomas may be present anywhere in the body and may not be visible at birth because of their small size or deep location. Some authors observe newborns usually present with isolated hemangiomas10. However, this condition can be considered a syndrome if the child shows others signs at birth11,12.

More than half of hemangiomas occur on the head and neck area and they range from a few millimeters to several centimeters in diameter3. In the oral cavity they appear more frequently on the gum, tongue and lips13. Epidemiological studies show that hemangiomas are more common in females than in males2,10. Likewise, their incidence is higher in low- birth- weight premature infants14,15.

The objective of this paper was to write a profile of children born with hemangiomas at Amaury de Medeiros Integrate Health Center (CISAM - Pernambuco, Brazil) between 1998 and 2008, analyze the prevalence of the condition and the following variables: gender, weight, prematurely, apgar score, location in the body and other malformations presence.

 

METHODS

Was realized descriptive analysis about gender, weight, prematurely, apgar score, hemangioma anatomic location and the presence of additional malformations obtained in medical records of newborns at CISAM, School Maternity Amaury de Medeiros Integrate Health Center, Brazil Northeast, between 1998 and 2008.

 

RESULTS

Out of 21.466 medical records examined, 68 were of children who showed a visible hemangioma in some location in the body, an incidence of 3.17 to 1.000 births. Thirty-eight (55.8%) of these newborns were female babies and 30 (44.2%), male babies. Weight analyses showed that 58 (85.2%) newborns displayed adequate weight, 08 (11.8%) showed low weight, 01 (1.5%) very low weight, 01 (1.5%) extremely low weight, and none showed overweight. Two (03%) of the children were born pre-term and sixty-six (97%) to term; none was post-term. The mean of the apgar score was 8. Sixty-two (91.2%) of the newborns presented normal apgar score at the first and fifth minutes after birth, 05 (7.3%) showed slight asphyxia, 01 (1.5%) moderate asphyxia and none serious asphyxia. Concerning location, 61 (89.7%) newborns presented hemangioma on the head and neck area; and six (8.8%) on other parts of the body. Location was not recorded for 01 (1.5%) child. Other malformations were identified in 15 (22%) of the newborns; none of the children was considered syndromic.

 

DISCUSSION

Results showed hemangiomas affected females most with ratio 1.2:12,3,15,16,17,18,19. These studies suggest female gender is more affected because of the hormonal factor. On the other hand, studies pointed that the condition has a slight female predilection20,21. Others showed hemangiomas displayed no clear predilection for gender10.

In our sample, 68 (92.6%) of all hemangiomas occurred in the cervicofacial region3,22,23,24 (Table 1). The locations most usually affected in this region in order of frequency are the nape of the neck, eyelid, glabellar region, and less commonly, the upper lip10. In our sample, in disagreement with this found .The eyelid was the most affected site 27 (39.7%). The involvements of the remaining sites, however, were in agreement with these authors: nape of the neck, 10 (14.7%); glabellar region, 07 (10.2%); and upper lip, 01 (1.4%). Twentythree (33.8%) of the hemangiomas were recorded on locations other than the cervicofacial region: the face (13 -19%), nose (05 -7.3%), tongue (01 -1.4%), lower lip (01 - 1.4%). Lips were the most often involved site, followed by the gingiva and tongue while the nose was never involved17. On the contrary, in our sample, the nose was more affected than the tongue and lips.

Capillary hemangiomas are more common in male patients with a ratio of 1.2:110. In the sample studied, only 03 female patients exhibited capillary hemangiomas with a sex ratio of 2:1. Authors also found that hemangiomas were more prevalent in trunk and extremities, followed by the head and neck10,17, whereas in this study, most cases involved the cervicofacial region except for 05 (7.3%) of them. In addition, in this study, there were cases of hemangiomas affecting more than one site and in one medical record; the location of the hemangioma was not mentioned.

Studies suggest that cutaneous hemangiomas on the nose, lip and parotid area, are slow to involute and just as likely to resolve as deep lesions3,23. Some of the children with cutaneous hemangiomas were born at term and had a normal apgar score .The apgar score is the measurement of a baby's physical condition and mental alertness evaluated at one and five minutes after birth. In our sample 62 (91.2%) children exhibited normal apgar score, mean score being 8. Sixty-six (97%) of the children were born to term, 02 (3%) were born pre-term and none was born post-term.

A great number of the newborns (65 out of 68 -95.5%) were born to term and with adequate weight at birth in disagreement some authors2,14,15,19. They show in your studies hemangiomas in low- weight premature babies (less than 1.500 grams ). Nevertheless there are authors that showed babies presented adequate weight at birth18,27. Only 02 (3%) of them weighted less than 1.500 grams10,26,28.

The presence of multiple hemangiomas on the face of a newborn may be a sign of Sturge-Weber Syndrome, an uncommon disorder. These lesions are called portwine nevus, usually affecting upper face ipsilateral to the angiomatosis. Other malformations may also be present such as leptomeningeal angiomatosis, seizures, glaucoma, mental retardations, when cutaneous malformation is unilateral or bilateral, including ophthalmic division of the trigeminal nerve7. In this study, out of a total of 68 cases of hemangiomas, 52 (76,4%) involved the face and none showed the characteristic signs of Sturge-Weber Syndrome. This data may be masked because our sample consisted of only 21.466 medical records and this syndrome is a rare disorder that occurs with a frequency of approximately 1 per 50.000 births11.

PHACE syndrome is another uncommon disorder that presents the acronym coined for this neurocutaneous syndrome which encompasses: Posterior fossa malformations of the brain, facial Hemangiomas, Arterial anomalies, Cardial anomalies and coarctation of aorta and Eye abnormalities4. Another disorder that includes the hemangioma as a residual tumor that persists in some cases is the Kasabach - Merritt Phenomenon. This is characterized by several thrombocytopenia, hypofibrinogenemia and microangiopathie hemolytic anemia15.

However, it is important to observe that most children who present with cutaneous vascular malformation do not have Sturge-Weber Syndrome, PHACE or Kasabach - Merritt Phenomenon5,12,29; the majority of patients present with a single, solitary, and well-circumscribed lesion3,10,15. Such was the case in 41 (60%) out of the 68 medical records checked in the present study.

Approximately 20% of the patients could present with more that one hemangioma3. Twenty-two out of 68 (32%) medical records examined confirmed this observation. There is a considerable controversy in determining how infants with multiples cutaneous hemangiomas should be evaluated so that the possibility of significant subcutaneous hemangiomas - deep lesions- could be detected3,10,12. Besides physical examination, some complementary exams such as ultrasound or magnetic resonances should be required in order to identify these lesions because the cell proliferations can affect the newborn body systems. In this research, no requirements of complementary exams in children with hemangiomas were found.

In Conclusions it was found that female babies were more susceptible to presenting with hemangiomas and that children who develop this nonmalignant tumor may have been born to term, with a normal apgar score, and adequate weight. A great number of newborns showed isolated lesions on the head and neck region without, however, other malformations suggestive of syndromes.

Epidemiological data on hemangiomas is still very controversial, which suggests the need of further studies on the subject.

 

ACKNOWLEDGEMENTS:

This investigation was supported by FACEPE/FDPEUPE. Many thanks to Mrs. Rejane Aquino de Lucena for the permission to use the Amaury de Medeiros Integrate Health Center archives.

 

REFERENCES

1. Mulliken JB, Glowacki J. Hemangiomas and vascular malformations in infants and children: a classification based on endothelial characteristics. Plast Reconstr Surg. 1982 Mar;69(3):412-22.         [ Links ]

2. Spring MA, Bentz ML. Cutaneous vascular lesions. Clin Plast Surg. 2005 Apr;32(2):171-86.         [ Links ]

3. Dinehart SM, Kincannon J, Geronemus R. Hemangiomas: evaluation and treatment. Dermatol Surg. 2001 May;27(5):475-85.         [ Links ]

4. Pascual-Castroviejo I. Vascular and nonvascular intracranial malformation associated with external capillary hemangiomas. Neuroradiology. 1978;16:82-4.         [ Links ]

5. Mohammadi M, Mohebbi MR, Holden KR. Facial hemangioma, and associated malformations: a case report. Neuropediatrics. 2004 Jun;35(3):194-7.         [ Links ]

6. Rodríguez CD. What is your assessment? Capillary hemangioma. Pediatr Nurs. 1998 MarApr;24(2):174-5.         [ Links ]

7. Baselga E. Sturge-Weber syndrome. Semin Cutan Med Surg. 2004 Jun;23(2):87-98.         [ Links ]

8. Blei F, Walter J, Orlow SJ, Marchuk DA. Familial segregation of hemangiomas and vascular malformations as an autosomal dominant trait. Arch Dermatol. 1998 Jun;134(6):718-22.         [ Links ]

9. Walter JW, Blei F, Anderson JL, Orlow SJ, Speer MC, Marchuk DA. Genetic mapping of a novel familial form of infantile hemangioma. Am J Med Genet. 1999 Jan 1;82(1):77-83.         [ Links ]

10. Conlon JD, Drolet BA. Skin lesions in the neonate. Pediatr Clin North Am. 2004 Aug;51(4):863-88, vii-viii.         [ Links ]

11. Garzon MC, Huang JT, Enjolras O, Frieden IJ. Vascular malformations. Part II: associated syndromes. J Am Acad Dermatol. 2007 Apr;56(4):541-64.         [ Links ]

12. Thomas-Sohl KA, Vaslow DF, Maria BL. Sturge-Weber syndrome: a review. Pediatr Neurol. 2004 May;30(5):303-10.         [ Links ]

13. Toida M, Hasegawa T, Watanabe F, Kato K, Makita H, Fujitsuka H, Kato Y, Miyamoto K, Shibata T, Shimokawa K. Lobular capillary hemangioma of the oral mucosa: clinicopathological study of 43 cases with a special reference to immunohistochemical characterization of the vascular elements. Pathol Int. 2003 Jan;53(1):1-7.         [ Links ]

14. Chiller KG, Passaro D, Frieden IJ. Hemangiomas of infancy: clinical characteristics, morphologic subtypes, and their relationship to race, ethnicity, and sex. Arch Dermatol. 2002 Dec;138(12):1567-76.         [ Links ]

15. Miller T, Frieden IJ. Hemangiomas: new insights and classification. Pediatr Ann. 2005 Mar;34(3):179-87.         [ Links ]

16. Mills SE, Cooper PH, Fechner RE. Lobular capillary hemangioma: the underlying lesion of pyogenic granulo-ma. A study of 73 cases from the oral and nasal mucous membranes. Am J Surg Pathol. 1980 Oct;4(5):470-9.         [ Links ]

17. Harris MN, Desai R, Chuang TY, Hood AF, Mirowski GW. Lobular capillary hemangiomas: An epidemiologic report, with emphasis on cutaneous lesions. J Am Acad Dermatol. 2000 Jun;42(6):1012-6.         [ Links ]

18. George ME, Sharma V, Jacobson J, Simon S, Nopper AJ. Adverse effects of systemic glucocorticosteroid therapy in infants with hemangiomas. Arch Dermatol. 2004 Aug;140(8):963-9.         [ Links ]

19. Hemangioma Investigator Group, Haggstrom AN, Drolet BA, Baselga E, Chamlin SL, Garzon MC, Horii KA, Lucky AW, Mancini AJ, Metry DW, Newell B, Nopper AJ, Frieden IJ. Prospective study of infantile hemangiomas: demographic, prenatal, and perinatal characteristics. J Pediatr. 2007 Mar;150(3):291-4.         [ Links ]

20. Kerr DA. Granuloma pyogenicum. Oral Surg Oral Med Oral Pathol. 1951Feb;4(2):158-76.         [ Links ]

21. Nkanza NK, Hutt MS. Pyogenic granuloma: a study of 181 cases from Malawi. East Afr Med J. 1981 May;58(5):318-23.         [ Links ]

22. Finn MC, Glowacki J, Mulliken JB. Congenital vascular lesion: clinical application of a new classification. J Pediatric Surg. 1983;18(6): 894-900.         [ Links ]

23. Weston WL, Lane AT. Neonatal Dermatology. In : T.B. Fitzpatrik AZE, Wolff, IMF, Austen KF. Dermatology in General Medicine. New York: McGraw-Hill; 1993. p.2941-60.         [ Links ]

24. Frieden IJ, Eichenfield LF, Esterly NB, Geronemus R, Mallory SB. Guidelines of care for hemangiomas of infancy. American Academy of Dermatology Guidelines/ Outcomes Committee. J Am Acad Dermatol. 1997 Oct;37(4):631-7.         [ Links ]

25. Redondo P. [Classification of vascular anomalies (tumours and malformations). Clinical characteristics and natural history]. An Sist Sanit Navar. 2004;27 Suppl 1:9-25.         [ Links ]

26. Drolet BA, Esterly NB, Frieden IJ. Hemangiomas in children. N Engl J Med. 1999 Jul 15;341(3):173-81.         [ Links ]

27. Von Bubnoff D, Bieber T, Steen K. Benign neonatal hemangiomatosis in a pre-term infant. J Dermatol. 2002 Aug;29(8):533-5.         [ Links ]

28. Bowers RE, Graham EA, Tomlinson KM. The natural history of Strawberry Nevus. Arch Dermatol. 1960; 82:667-80.         [ Links ]

29. Tallman B, Tan OT, Morelli JG, Piepenbrink J, Stafford TJ, Trainor S, Weston WL. Location of portwine stains and the likelihood of ophthalmic and/or central nervous system complications. Pediatrics. 1991 Mar;87(3):323-7.         [ Links ]

 

 

Corresponding author:
Ana Paula Veras Sobral
Rua Monte Alverne, 107/05, Hipódromo
Recife - PE / Brasil. CEP: 52.041-610
Fax: + 55 81 3458-6758
E-mail address: anapvsobral@hotmail.com, ana-pavsobral@yahoo.com.br

Recebido em 15/12/2009
Aprovado em 03/03/2010