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Arquivos de Neuro-Psiquiatria

Print version ISSN 0004-282XOn-line version ISSN 1678-4227

Arq. Neuro-Psiquiatr. vol.66 no.2b São Paulo June 2008

http://dx.doi.org/10.1590/S0004-282X2008000300029 

CLINICAL/SCIENTIFIC NOTES

 

Shapiro syndrome with hypothalamic hypothyroidism

 

Síndrome de Shapiro assoociado a hipotireoidismo hipotalâmico

 

 

Ronaldo ArkaderI; Carlos Augusto TakeuchiII

IMD, Pediatrician
IIMD, Child Neurologist

 

 

Shapiro syndrome, first described in 1969, is an extremely rare condition consisting of the clinical triad of recurrent hypothermia, sweating, and chills in the presence of agenesis of the corpus callosum. The periodicity of the hypothermic episodes ranges from hours to years, and episodes may last hours to weeks. Typically, but not invariably, there are associated central nervous system abnormalities affecting structures, particularly in the hypothalamus1. Central forms of hypothyroidism include secondary hypothyroidism, which is caused by TSH deficiency, and tertiary hypothyroidism, which is caused by TRH deficiency2.

We describe a previously healthy boy with Shapiro syndrome and hypothalamic hypothyroidism treated with thyroxine and cyproheptadine.

 

CASE

A 8-year-old boy in otherwise good health, who, since 5 years of age, presented with sporadic episodes of nocturnal hypothermia, associated with pallor and profuse sweating. The axillary body temperature during the episodes was 34.5ºC, lasting for approximately an hour. The episodes recurred 10 or 12 times a month during sleep. Blood analysis indicated a normal complete blood count and blood chemistry. Morning cortisol (am), prolactin, growth hormone, LH and FSH were also normal for age. Thyroid stimulating hormone was 4.8 µU/mL (normal range 0.4 to 4.0), free thyroxine (FT4) was 1.3 µIU/mL (range 4-56). After exclude other causes of hipothyreoidism we performed a TRH stimulation test for the differentiation of hypothalamic from pituitary disease. Plasma TSH was measured before and 15, 30, 45, 60, 120, and 180 min after iv administration of TRH (10 µg·kg-1) An adequate TSH response to TRH was defined by a peak concentration exceeding 15 µU/ml and return to baseline within 3 h. A TRH test demonstrated an blunted response (TSH: basal 2.1 µU/mL and a peak 4.3 µU/mL - deltaTSH <4.5) Hypothalamic morphology was assessed using magnetic resonance imaging (MRI) (Figure).

 

 

The child mother signed the informed consent for publish the case

 

DISCUSSION

The majority of pediatric cases of hypothermia, defined as a core body temperature below 35ºC, are caused by environmental exposures. Nonenvironmental hypothermia in pediatric patients is uncommon. Life-threatening causes of nonenvironmental hypothermia include sepsis, drug ingestions, brain tumors, and endocrinologic abnormalities. Cyproheptadine, an antiserotonergic medication, has been shown to abort or control these episodes in some patients1.

The symptoms of central hypothyroidism include fatigue, apathy, weight gain, dry skin, constipation and cold intolerance deficiency of TRH secretion gives rise to hypothalamic hypothyroidism, also called tertiary hypothyroidism, which can occur in hypothalamic disease or more rarely as an isolated defect. Hypothalamic and pituitary causes of TSH deficiency are most readily distinguished by imaging methods. Although theoretically reasonable, the TRH stimulation test for the differentiation of hypothalamic disease from pituitary disease is of limited value. The typical pituitary response to TRH administration in patients with TRH deficiency is an enhanced and somewhat delayed peak, whereas the response with pituitary failure is subnormal or absent. Low free T4 without elevated TSH is consistent with central hypothyroidism2,3. We started thyroxine and cyproheptadine, and after one month the patient symptoms disappeared. We emphasize the importance of recognition the syndrome and associated endocrine manisfestations and the current treatment.

 

REFERENCES

1. Sheth RD, Barron TF, Hartlage PL. Episodic spontaneous hypothermia with hyperhidrosis: implications for pathogenesis. Pediatr Neurol 1994;10:58-60.         [ Links ]

2. Gruñeiro de Papendieck L, Iorcansky S, Rivarola MA, Heinrich JJ, Bergadá C. Patterns of TSH response to TRH in children with hypopituitarism. J Pediatr 1982;100:387-392.         [ Links ]

3. Rapaport R, Sills I, Patel U, et al. Thyrotropin-releasing hormone stimulation tests in infants. J Clin Endocrinol Metab 1993;77:889-894.         [ Links ]

 

 

Received 17 August 2007. Accepted 22 April 2008.

 

 

Dr. Ronaldo Arkader - Department of Pediatric Intensive Care, Hospital Sabará - Rua Dona Antonia de Queiros 505 - 01307-010 São Paulo SP - Brasil. E-mail: r-arkader@uol.com.br

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