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1.
J Pediatr Adolesc Gynecol ; 37(4): 448-450, 2024 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-38278410

RESUMEN

BACKGROUND: Lichen sclerosus (LS) is a chronic inflammatory disorder, presenting with pruritis and hypopigmentation of the vulvar and anogenital skin. LS presenting as a peri-clitoral mass has not been previously described. CASE: A 5-year-old patient with vulvar pruritis and ultrasound showing a homogenous mass was referred for suspected clitoromegaly with normal labs. Examination demonstrated a prepubertal patient with a mobile, soft, peri-clitoral mass and surrounding hypopigmentation consistent with LS. The cyst was excised surgically; pathology revealed an epidermal inclusion cyst. Postoperatively, she began using topical steroids for LS with symptom resolution. CONCLUSION: Thorough workup of clitoromegaly negative for hormonal causes requires further investigation to determine an alternative etiology of the mass. We suspect that inflammatory changes of LS and pruritus resulted in the peri-clitoral inclusion cyst.


Asunto(s)
Clítoris , Quiste Epidérmico , Humanos , Femenino , Preescolar , Quiste Epidérmico/cirugía , Quiste Epidérmico/complicaciones , Quiste Epidérmico/diagnóstico , Quiste Epidérmico/diagnóstico por imagen , Quiste Epidérmico/patología , Clítoris/patología , Liquen Escleroso y Atrófico/complicaciones , Liquen Escleroso y Atrófico/diagnóstico , Liquen Escleroso Vulvar/complicaciones , Liquen Escleroso Vulvar/diagnóstico , Enfermedades de la Vulva/etiología , Enfermedades de la Vulva/cirugía , Enfermedades de la Vulva/diagnóstico
2.
J Pediatr Adolesc Gynecol ; 37(1): 67-71, 2024 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-37704034

RESUMEN

BACKGROUND: Rubinstein-Taybi syndrome (RSTS) is a multi-system neurodevelopmental condition caused by deficiency of CREBBP (16p13.3) or EP300 (22q13.2). Müllerian agenesis, or Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, is defined as congenital agenesis of the uterus, cervix, and upper vagina without a definite genetic cause. INDEX CASE AND CASE SERIES: We present a 14-year-old female with RSTS type 1 (CREBBP, c.4395-2A>C) and MRKH, the first documented in the literature. Following presentation to Gynecology for anticipatory guidance regarding future menstrual suppression and follow-up of previously diagnosed labial adhesions, exam under anesthesia revealed a single urogenital opening with cystoscopy demonstrating a normal urethra and bladder. Laboratory evaluation was consistent with peripubertal female gonadotropins and estradiol, 46,XX karyotype, and normal microarray, and a pelvic MRI confirmed Müllerian agenesis. Given this case, we assessed our cohort of females with RSTS and found that 4 of 12 individuals also had Müllerian anomalies. CONCLUSION: Gynecologic evaluation should be a part of medical care for females with RSTS, particularly in individuals with delayed menarche or abnormal menstrual history, on the basis of the observed association between RSTS and Müllerian anomalies in this case series. Although several candidate genes and copy number variants are associated with MRKH, no candidate genes in close proximity to the 16p13.3 region have been identified to explain both RSTS and MRKH in the index patient. Due to the regulatory nature of CREBBP during embryonic development, we theorize that CREBBP may play a role in the migration of Müllerian structures during embryogenesis.


Asunto(s)
Trastornos del Desarrollo Sexual 46, XX , Productos Biológicos , Anomalías Congénitas , Síndrome de Rubinstein-Taybi , Femenino , Humanos , Adolescente , Síndrome de Rubinstein-Taybi/genética , Vagina/anomalías , Trastornos del Desarrollo Sexual 46, XX/diagnóstico , Conductos Paramesonéfricos/anomalías , Anomalías Congénitas/genética , Anomalías Congénitas/diagnóstico
3.
J Pediatr Surg ; 58(12): 2300-2307, 2023 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-37690871

RESUMEN

STUDY OBJECTIVE: Long-term gynecologic data are lacking to inform the care of patients with cloacal malformations. We seek to examine perceived sexual and reproductive health challenges of patients born with cloacal anomalies and characterize the experiences of patients as adults. DESIGN AND SETTING: Virtual semi-structured focus groups and single-participant interviews were conducted using an online video platform. Retrospective chart review was performed to abstract available demographics and surgical history. PARTICIPANTS: Adult patients were contacted from a database of 143 patients born with cloaca who had been seen at or referred to a tertiary care pediatric colorectal center. Participants were recruited until data collection reached thematic saturation. Twenty patients aged 18-53 years participated in 5 focus groups and 3 single-participant interviews. The hospital IRB determined the research activities to be exempt from IRB review and oversight. INTERVENTIONS AND MAIN OUTCOME MEASURES: Interviews and focus groups were transcribed and analyzed using the constant comparative method to identify themes regarding sexual and reproductive health and compared with medical and surgical history abstracted from chart review. RESULTS: Participants reported many perceived barriers to intercourse and intimacy including bowel and bladder continence management. All participants reported discussion of pregnancy and fertility with healthcare providers as important. Other common themes included concerns about independence and transitioning from pediatric to adult providers. CONCLUSION: Anorectal malformations are associated with sexual and reproductive health concerns. Patients seek guidance on family building, intimacy, and transition to adult care. Future quantitative study of these topics is needed to develop best practices for counseling and clinical management of these patients. LEVEL OF EVIDENCE: Level VI. TYPE OF STUDY: Prognosis Study.


Asunto(s)
Malformaciones Anorrectales , Cloaca , Embarazo , Animales , Humanos , Adulto , Femenino , Niño , Estudios Retrospectivos , Cloaca/anomalías , Salud Reproductiva , Malformaciones Anorrectales/complicaciones , Conducta Sexual , Investigación Cualitativa
4.
Brain ; 133(Pt 12): 3764-77, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-21081551

RESUMEN

Impaired consciousness requires altered cortical function. This can occur either directly from disorders that impair widespread bilateral regions of the cortex or indirectly through effects on subcortical arousal systems. It has therefore long been puzzling why focal temporal lobe seizures so often impair consciousness. Early work suggested that altered consciousness may occur with bilateral or dominant temporal lobe seizure involvement. However, other bilateral temporal lobe disorders do not impair consciousness. More recent work supports a 'network inhibition hypothesis' in which temporal lobe seizures disrupt brainstem-diencephalic arousal systems, leading indirectly to depressed cortical function and impaired consciousness. Indeed, prior studies show subcortical involvement in temporal lobe seizures and bilateral frontoparietal slow wave activity on intracranial electroencephalography. However, the relationships between frontoparietal slow waves and impaired consciousness and between cortical slowing and fast seizure activity have not been directly investigated. We analysed intracranial electroencephalography recordings during 63 partial seizures in 26 patients with surgically confirmed mesial temporal lobe epilepsy. Behavioural responsiveness was determined based on blinded review of video during seizures and classified as impaired (complex-partial seizures) or unimpaired (simple-partial seizures). We observed significantly increased delta-range 1-2 Hz slow wave activity in the bilateral frontal and parietal neocortices during complex-partial compared with simple-partial seizures. In addition, we confirmed prior work suggesting that propagation of unilateral mesial temporal fast seizure activity to the bilateral temporal lobes was significantly greater in complex-partial than in simple-partial seizures. Interestingly, we found that the signal power of frontoparietal slow wave activity was significantly correlated with the temporal lobe fast seizure activity in each hemisphere. Finally, we observed that complex-partial seizures were somewhat more common with onset in the language-dominant temporal lobe. These findings provide direct evidence for cortical dysfunction in the form of bilateral frontoparietal slow waves associated with impaired consciousness in temporal lobe seizures. We hypothesize that bilateral temporal lobe seizures may exert a powerful inhibitory effect on subcortical arousal systems. Further investigations will be needed to fully determine the role of cortical-subcortical networks in ictal neocortical dysfunction and may reveal treatments to prevent this important negative consequence of temporal lobe epilepsy.


Asunto(s)
Corteza Cerebral/fisiopatología , Trastornos de la Conciencia/fisiopatología , Epilepsia del Lóbulo Temporal/fisiopatología , Convulsiones/fisiopatología , Adulto , Conducta/fisiología , Ritmo beta , Trastornos de la Conciencia/etiología , Ritmo Delta , Electrodos Implantados , Electroencefalografía , Epilepsias Parciales/complicaciones , Epilepsias Parciales/fisiopatología , Epilepsia Parcial Compleja/complicaciones , Epilepsia Parcial Compleja/fisiopatología , Epilepsia del Lóbulo Temporal/complicaciones , Femenino , Humanos , Masculino , Persona de Mediana Edad , Neocórtex/fisiopatología , Convulsiones/complicaciones , Adulto Joven
5.
Case Rep Womens Health ; 30: e00301, 2021 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-33680870

RESUMEN

BACKGROUND: Of women diagnosed with endometriosis, 3.8-37% have bowel endometriosis. The cecum is the least common site for endometriotic implants affecting the bowel, accounting for only 3.6-6% of cases. We present a case of intrauterine fetal demise at term in which the patient was found to have gastrointestinal bleeding caused by endometriosis of the cecum. CASE: A 35-year-old woman, gravida 4, para 1, at 37 weeks and 3 days of gestation, without a known history of endometriosis but with two prior miscarriages, presented with severe anemia and intrauterine fetal demise. During delivery, melanotic stool was noted. Colonoscopic biopsy noted the source of bleeding to be a 2 cm endometriotic implant in the patient's cecum. Suppression therapy was started. Postpartum, the patient underwent laparoscopic cecectomy and pathology confirmed the diagnosis of endometriosis. CONCLUSION: Hemorrhage from endometriotic implants may occur during pregnancy due to changes in the hormonal milieu. Bowel endometriosis may increase the risk of maternal hemorrhage during pregnancy, thereby increasing the risk of unfavorable pregnancy outcomes, including intrauterine fetal demise.

6.
Ann N Y Acad Sci ; 1157: 48-60, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19351355

RESUMEN

Although the precise mechanisms for control of consciousness are not fully understood, emerging data show that conscious information processing depends on the activation of certain networks in the brain and that the impairment of consciousness is related to abnormal activity in these systems. Epilepsy can lead to transient impairment of consciousness, providing a window into the mechanisms necessary for normal consciousness. Thus, despite differences in behavioral manifestations, cause, and electrophysiology, generalized tonic-clonic, absence, and partial seizures engage similar anatomical structures and pathways. We review prior concepts of impaired consciousness in epilepsy, focusing especially on temporal lobe complex partial seizures, which are a common and debilitating form of epileptic unconsciousness. We discuss a "network inhibition hypothesis" in which focal temporal lobe seizure activity disrupts normal cortical-subcortical interactions, leading to depressed neocortical function and impaired consciousness. This review of the major prior theories of impaired consciousness in epilepsy allows us to put more recent data into context and to reach a better understanding of the mechanisms important for normal consciousness.


Asunto(s)
Trastornos de la Conciencia/etiología , Epilepsia/complicaciones , Trastornos de la Conciencia/diagnóstico , Trastornos de la Conciencia/fisiopatología , Trastornos de la Conciencia/psicología , Epilepsia/fisiopatología , Epilepsia/psicología , Epilepsia Parcial Compleja/complicaciones , Epilepsia Parcial Compleja/fisiopatología , Epilepsia Parcial Compleja/psicología , Epilepsia del Lóbulo Temporal/complicaciones , Epilepsia del Lóbulo Temporal/fisiopatología , Epilepsia del Lóbulo Temporal/psicología , Lateralidad Funcional/fisiología , Humanos , Modelos Neurológicos , Modelos Psicológicos , Neocórtex/fisiopatología , Red Nerviosa/fisiopatología , Tomografía Computarizada de Emisión de Fotón Único
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