Javascript must be enabled to continue!
Isolated Absent Thelarche in a Patient With Neurofibromatosis Type 1 and Acromegaly
View through CrossRef
BACKGROUND:
Isolated absent thelarche is a rare condition that is infrequently reviewed in the literature.
CASE:
A 28-year-old woman with neurofibromatosis type 1 and acromegaly presented with absent breast development despite hormone therapy. Examination noted a normally developed woman with acromegalic features and Tanner stage I breasts. Hormone studies and karyotype were normal. Magnetic resonance imaging of the patient's brain demonstrated a voluminous pituitary. Chromosome microarray analysis diagnosed the neurofibromatosis 1 microdeletion syndrome. Breast ultrasonography and surgical consultation were offered.
CONCLUSIONS:
Neither neurofibromatosis type 1, acromegaly, nor neurofibromatosis 1 microdeletion syndrome are linked to absent thelarche. After attempting hormone therapy, patients with absent thelarche should be evaluated for congenital breast anomalies, estrogen receptor abnormalities, or gene defects. Psychological and surgical consultation should also be offered.
Ovid Technologies (Wolters Kluwer Health)
Title: Isolated Absent Thelarche in a Patient With Neurofibromatosis Type 1 and Acromegaly
Description:
BACKGROUND:
Isolated absent thelarche is a rare condition that is infrequently reviewed in the literature.
CASE:
A 28-year-old woman with neurofibromatosis type 1 and acromegaly presented with absent breast development despite hormone therapy.
Examination noted a normally developed woman with acromegalic features and Tanner stage I breasts.
Hormone studies and karyotype were normal.
Magnetic resonance imaging of the patient's brain demonstrated a voluminous pituitary.
Chromosome microarray analysis diagnosed the neurofibromatosis 1 microdeletion syndrome.
Breast ultrasonography and surgical consultation were offered.
CONCLUSIONS:
Neither neurofibromatosis type 1, acromegaly, nor neurofibromatosis 1 microdeletion syndrome are linked to absent thelarche.
After attempting hormone therapy, patients with absent thelarche should be evaluated for congenital breast anomalies, estrogen receptor abnormalities, or gene defects.
Psychological and surgical consultation should also be offered.
Related Results
Autonomy on Trial
Autonomy on Trial
Photo by CHUTTERSNAP on Unsplash
Abstract
This paper critically examines how US bioethics and health law conceptualize patient autonomy, contrasting the rights-based, individualist...
The acromegaly lipodystrophy
The acromegaly lipodystrophy
Growth hormone (GH) and insulin-like growth factor 1 (IGF-1) are essential to normal growth, metabolism, and body composition, but in acromegaly, excesses of these hormones striki...
Incidence of bronchiectasis in patients with acromegaly: a cohort study
Incidence of bronchiectasis in patients with acromegaly: a cohort study
ObjectiveAssociations between acromegaly and several respiratory diseases, such as obstructive lung disease or sleep apnea, have been suggested, but the relationship between bronch...
Functional and structural evaluation of hearing in acromegaly
Functional and structural evaluation of hearing in acromegaly
SummaryContext The impact of acromegaly on the auditory system remains unknown.Objective This study aimed to examine audiological symptoms and the structure and function of the a...
Growth hormone and insulin-like growth factor 1 affect the severity of Graves’ disease
Growth hormone and insulin-like growth factor 1 affect the severity of Graves’ disease
Summary
Graves’ disease, the most common form of hyperthyroidism in iodine-replete countries, is associated with the presence of immunoglobulins G (IgGs) that are responsible for t...
NEUROFIBROMATOSIS COMPLICATED BY INTRACRANIAL TUMORS
NEUROFIBROMATOSIS COMPLICATED BY INTRACRANIAL TUMORS
Four cases of neurofibromatosis complicated by intracranial tumors are reported. Case 1 showed an intracranial neurofibromatosis while the other three cases contained gliomas in va...
Neurosurgical Presentations of Neurofibromatosis Type 1: Our Experience in a Regional Neurosurgical Centre, Sokoto, Nigeria
Neurosurgical Presentations of Neurofibromatosis Type 1: Our Experience in a Regional Neurosurgical Centre, Sokoto, Nigeria
Objective: The objective of this paper was to highlight various neurosurgical presentations of patients with neurofibromatosis type 1 seen in our center.
Design: This is retrospect...
Are We Achieving Pharmacological Disease Control in Acromegaly?
Are We Achieving Pharmacological Disease Control in Acromegaly?
Acromegaly is a rare endocrine disorder, associated with significant morbidity and mortality due to the harmful effects of prolonged exposure to increased levels of growth hormone ...

