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1.
Pan Afr Med J ; 33: 286, 2019.
Article in English | MEDLINE | ID: mdl-31692884

ABSTRACT

Cyclic vomiting syndrome (CVS) is defined by episodes of vomiting lasting from a few hours to several days, alternating with periods of no symptoms. Various symptoms can be associated with vomiting such as nausea, migraine or abdominal pain. Common triggers of CVS include infection, psychological stress and menstruation. CVS's diagnosis requires exclusion of alternative diseases particularly neurological and gastrointestinal. CVS shares many common features with catamenial migraine including treatment. We herein report a case of CVS in a 16 years old girl characterized by stereotypical vomiting attacks occurring in every menstrual period. Recurrent vomiting episodes began 2 years before admission. Given the negativity of paraclinical exams and the absence of response to different therapeutic approaches as well as the similarity with catamenial migraine, we treated our patient with permenstrual percutaneous oestrogen for six months. The evolution was marked by the disappearance of symptoms within the first month and the absence of their recurrence after treatment cessation during a follow-up of 6 years.


Subject(s)
Estrogens/administration & dosage , Menstrual Cycle/physiology , Vomiting/drug therapy , Adolescent , Female , Follow-Up Studies , Humans , Treatment Outcome
2.
J Coll Physicians Surg Pak ; 29(12): S101-S102, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31779756

ABSTRACT

Kallmann syndrome is a rare genetic disorder marked by hypogonadotropic hypogonadism (HH) and anosmia, affecting 1 in 50,000 females. It is due to a defect of gonadotropin-releasing hormone (GnRH)-secreting neurons migration from the nasal olfactory epithelium to the basal hypothalamus. Non-reproductive, non-olfactory symptoms can also be present, depending on the genetic form of disease. The management includes hormone replacement therapy and fertility treatment. We report a case of Kallmann syndrome in an 18-year girl who presented with primary amenorrhea with poor, secondary sexual characteristics' development, poor sense of smell and syndactyly. The plasma levels of luteinising hormone, follicle stimulating hormone, and estradiol were very low, while chromosome analysis showed 46, XX karyotype. Pelvic MRI confirmed the presence of uterus and ovaries. MRI of brain was normal. Treatment was started with cyclic conjugated estrogen and progestin with good response. She is now on regular follow-up to monitor treatment.


Subject(s)
Abnormalities, Multiple , Kallmann Syndrome/diagnosis , Syndactyly/diagnosis , Adolescent , Biomarkers/blood , Female , Gonadotropin-Releasing Hormone/blood , Humans , Kallmann Syndrome/blood , Luteinizing Hormone/blood , Magnetic Resonance Imaging
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