Disorders of sex development (DSDs) are congenital conditions in which the development of chromosomal, gonadal, or anatomic sex is atypical. DSDs can be classified broadly into four categories on the basis of gonadal histologic features: female pseudohermaphroditism (46,XX with two ovaries); male pseudohermaphroditism (46,XY with two testes); true hermaphroditism (ovotesticular DSD) (both ovarian and testicular tissues); and gonadal dysgenesis, either mixed (a testis and a streak gonad) or pure (bilateral streak gonads). Imaging plays an important role in demonstrating the anatomy and associated anomalies. Ultrasonography is the primary modality for demonstrating internal organs; genitography is used to assess the urethra, vagina, and any fistulas or complex tracts; and magnetic resonance imaging is used as an adjunct modality to assess for internal gonads and genitalia. Early and appropriate gender assignment is necessary for healthy physical and psychologic development of children with ambiguous genitalia. Gender assignment can be facilitated with a team approach that involves a pediatric endocrinologist, geneticist, urologist, psychiatrist, social worker, neonatologist, nurse, and radiologist, allowing timely diagnosis and proper management.

Every major vessel in the human body has a characteristic flow pattern that is visible in spectral waveforms obtained in that vessel with Doppler ultrasonography (US). Spectral waveforms reflect the physiologic status of the organ supplied by the vessel, as well as the anatomic location of the vessel in relation to the heart. In addition, the waveforms may be affected by age- and development-related hemodynamic differences. For example, adults tend to have higher flow velocities, whereas neonates, particularly those born prematurely, have higher resistance to flow, especially in the cerebral and renal vascular beds. As Doppler US is performed with increasing frequency for vascular evaluation in children, the recognition of normal flow patterns has become imperative. Familiarity with the waveforms characteristic of specific veins and arteries in children is important. In addition, an understanding of the hemodynamic factors involved provides a useful basis for interpreting waveform abnormalities.

BACKGROUND: Thyroid malignancy is rare in young children, although the incidence increases sharply during adolescence. Nodular thyroid disease and thyroid cancer in children differ substantially from those in adults, because the rates of malignancy among children are roughly 5‐fold higher, and local and distant metastases as well as recurrences are more common. Even with the recent introduction of pediatric guidelines, there remains a paucity of pediatric data on which to base clinical decision making. The objectives of this study were to characterize the outcomes of fine‐needle aspiration biopsy (FNAB) of nodular thyroid disease at a pediatric tertiary‐care institution over a 24‐year period and to relate cytopathology to histopathology and management decisions in this population.METHODS: A retrospective review of patients who underwent preoperative FNAB and thyroid surgery between 1992 and 2015 was conducted. In total, 207 nodules were biopsied among 178 patients.RESULTS: Adequate FNAB samples were obtained in 74% of biopsies. Sixty‐five patients underwent thyroidectomy after FNAB. In this group, the malignancy rates for lesions deemed benign, atypical, suspicious, and malignant on FNAB cytology were 16%, 67%, 71%, and 100%, respectively. Twenty‐seven individuals underwent >1 biopsy; however, no malignancies were identified in these patients. Surprisingly, the rate of malignancy in patients who underwent preoperative FNAB was not significantly different from the rate in those who proceeded directly to surgery (n = 146).CONCLUSIONS: FNAB remains a valuable tool for preoperative assessment of pediatric thyroid nodules. When samples are adequate for assessment, cytology other than clearly “benign” merits referral for diagnostic or therapeutic thyroidectomy. In this series, FNAB did not reduce rates of surgery for benign disease. Cancer Cytopathol 2016;124:801‐10. © 2016 American Cancer Society.

Sialorrhea is defined as the involuntary, passive pooling and spillage of saliva from the mouth due to the inability to process oral secretions. Although it is common in children who have not developed oral neuromuscular control (younger than 24 months), drooling in individuals 4 years or older is considered abnormal.^1-4 Patients with neurologic disorders such as Bell palsy, mental retardation, and cerebral palsy often experience excessive drooling.⁵ In children diagnosed as having cerebral palsy, it is estimated that 10% to 37% have sialorrhea.^5,6