Extensive hyperpigmentation during pregnancy: a case report

نویسندگان

  • Anthony Massinde
  • Salvatore Ntubika
  • Moke Magoma
چکیده

INTRODUCTION Skin hyperpigmentation is common during pregnancy and often is due to endocrinological changes. Usual patterns include linea nigra, darkening of areola and melasma. We report a rare diffused hyperpigmentation condition in a pregnant woman of dark colored skin. CASE PRESENTATION A 19-year-old Tanzanian primigravida at 32 weeks gestation presented at our antenatal clinic concerned about an insidious but progressive onset of unusual darkening of her abdominal skin and both breasts. Her antenatal record was unremarkable except for this unusual onset of abnormal skin color. Findings from her physical examination were unremarkable, and she had a normal blood pressure of 120/70 mmHg. Her abdomen was distended with a uterine fundus of 34 weeks. Almost her entire abdominal skin had darkly colored diffuse deep hyperpigmentation extending cephalad from both iliac fossae to involve both breasts to 2-3 cm beyond the areolae circumferentially. She had a fetus in longitudinal lie and cephalic presentation, with a normal fetal heart rate of 140 beats per minute. Other examination findings were unremarkable. The impression at this stage was exaggerated pigmentation of pregnancy. No medical treatment was offered but she was counseled that she might need medical treatment after delivery. She progressed well and had spontaneous labor and normal delivery at 38 weeks gestation. She was lost to follow up. CONCLUSION Unusual pregnancy-related skin hyperpigmentation can occur with no adverse consequences to pregnancy, although may worry a pregnant woman. Reassurance and conservative management may be all that is required to allay a patient's concerns.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

P-96: Extensive Fundal Uterine Rupture in Post-resection Bicornuate Uterus in a Term Pregnancy: A Case Report

Background Uterine rupture in a term pregnancy is an adverse and rare event with serious maternal and fetal consequences. The history of uterine septum resection is considered as a risk factor for uterine rupture. Women with such circumstances are thus recommended to be considered as having a high-risk pregnancy. Accordingly, their prenatal care should be implemented in shorter intervals during...

متن کامل

Acquired universal melanosis (Carbon baby syndrome) in a 4-year old girl

Universal acquired melanosis is a rare cause of diffuse hyperpigmentation of skin and mucosa during childhood. There are only few reported case of this scarce syndrome in medical literature. We report the first case of universal acquires melanosis from Iran in a 4-year-old girl whose skin becomes darker after 2-month of age.

متن کامل

Congenital Chikungunya with Centro-facial Pigmentation and Persistent Thrombocytopenia: A Case Report

Hyperpigmentation over face in a neonate is rare and the differentials for the same are also rare. Congenital chickengunya, fungal and viral infections, drug rash are few differentials. Chikungunya virus (CHIKV) infection manifesting in neonates is very rare. The prevalence of the entity was described only recently. We describe a neonate with hyperpigmentation on day 3 of life with stormy cours...

متن کامل

Segmental Speckled Lentiginous Nevus Exacerbated by Pregnancy in an Otherwise Healthy Female: A Case Report

Speckled lentiginous nevi (SLN), or nevus spili, are seen in 0.2% to 2.3% of the population, presenting as tan patches with overlying hyperpigmented macules or papules in a speckled arrangement. Segmental SLN represent a small subset of SLN, with the segmental type comprised of larger, unilateral lesions that may rarely give rise to melanomas and have been reported to proliferate in response to...

متن کامل

Congenital Becker’s nevus: report of a rare case

Introduction: Beckers’s nevus is a cutaneous hamartoma which usually appears as a circumscribed hyperpigmentation with hypertrichosis. It usually presents unilaterally and the usual site is shoulder and scapula. It is rarely congenital and it is usually noticed first during adolescence. Case Report: Herein, we report a congenital bilateral large Becker’s nevus with positive familial history ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 5  شماره 

صفحات  -

تاریخ انتشار 2011