A Case Report on Full Term Broad Ligament Pregnancy

2021 ◽  
pp. 89-93
Author(s):  
Vidhi J. Shah
Keyword(s):  
Case Report ◽  
Broad Ligament ◽  
Full Term

Broad ligament pregnancy with pelvic congestion syndrome: A case report

2021 ◽  
Author(s):  
Ruyue Ma ◽  
Junhua Guan ◽  
Jina Chen ◽  
Ke Sun ◽  
Liwen Zhang ◽  
...  
Keyword(s):  
Case Report ◽  
Broad Ligament ◽  
Pelvic Congestion Syndrome ◽  
Pelvic Congestion

scholarly journals Severe acquired cytomegalovirus infection in a full-term, formula-fed infant: Case Report

2011 ◽  
Vol 11 (1) ◽  
Author(s):  
Alberto Berardi ◽  
Cecilia Rossi ◽  
Valentina Fiorini ◽  
Cristina Rivi ◽  
Federica Vagnarelli ◽  
...  
Keyword(s):  
Case Report ◽  
Cytomegalovirus Infection ◽  
Full Term ◽  
Infant Case

The Weismann-Netter Syndrome: A Cause of Bowed Legs in Childhood

PEDIATRICS ◽  
1991 ◽  
Vol 88 (2) ◽  
pp. 334-337
Author(s):  
GARY L. FRANCIS ◽  
JAMES J. JELINEK ◽  
KATHLEEN MCHALE ◽  
MEGAN ADAMSON ◽  
SONDRA W. LEVIN
Keyword(s):  
Case Report ◽  
Short Stature ◽  
Skeletal Dysplasia ◽  
Full Term ◽  
Pediatric Age ◽  
Uncomplicated Pregnancy ◽  
Age Range

The Weismann-Netter syndrome is a rare, heritable skeletal dysplasia which often presents as asymptomatic bowing of the lower legs or short stature.1 Although more than 40 cases have been described, there is mention of only 8 cases in patients who were younger than 16 years of age.1-9 In retrospect, most of the affected adults reported symptoms during childhood. We recently had the opportunity to evaluate a 4-year-old boy, whom we believe to have the Weismann-Netter syndrome. This case served to heighten our awareness of this condition, which should be recognizable in the pediatric age range. CASE REPORT The proband (Fig 1), a four-year-old Arabic boy, was the product of a full-term, uncomplicated pregnancy.

Letters to the Editor

PEDIATRICS ◽  
1973 ◽  
Vol 51 (2) ◽  
pp. 311-312
Author(s):  
L. Michael Fiengold
Keyword(s):  
Case Report ◽  
Term Infant ◽  
Full Term ◽  
X Rays ◽  
Letters To The Editor ◽  
Meconium Aspiration ◽  
Full Term Infant

The case reported by Drs. Keidel and Feingold of Wilson Mikity Disease in a full-term infant indeed had meconium aspiration as a component. However, the baby went on to have oxygen dependency for at least a month following birth. This of course differs entirely from the syndrome of meconium aspiration. Moreover, the case was reviewed by Dr. Arnold Rudolph and Dr. Victor Mikity who read the x-rays personally. There is no doubt that the case report is valid and can clearly be differentiated from the course of the two infants that Dr. Cohen reported.

NEONATAL NECROTIZING ENTEROCOLITIS—OLD PIT-FALL OR NEW PROBLEM?

PEDIATRICS ◽  
1971 ◽  
Vol 48 (3) ◽  
pp. 345-348
Author(s):  
George H. Fetterman
Keyword(s):  
Case Report ◽  
Clinical Diagnosis ◽  
Necrotizing Enterocolitis ◽  
Early Stage ◽  
Newborn Infants ◽  
Full Term ◽  
European Literature ◽  
Original Case ◽  
Neonatal Necrotizing Enterocolitis

No pediatrician with responsibility for the care of newborn infants, premature or full term, can fail to be interested in the syndrome of neonatal necrotizing enterocolitis. The recent outpouring of reports concerning the disease attests not only to the growing recognition of the problem but also the immediacy of the challenge which it presents. The challenge is twofold, demanding clinical diagnosis of the disease at an early stage as well as study directed toward the elucidation of its etiology and pathogenesis. The most quoted articles from the European literature are Genersich's1 original case report in 1891, the series of 62 cases described by Willi2 in 1944, and the series reported by Rossier, et al.3 in 1959.

Uterine-like Mass With Features of an Extrauterine Adenomyoma Presenting 22 Years After Total Abdominal Hysterectomy–Bilateral Salpingo-oophorectomy: A Case Report and Review of the Literature

2005 ◽  
Vol 129 (8) ◽  
pp. 1041-1043 ◽  
Author(s):  
Rachel Redman ◽  
Edward J. Wilkinson ◽  
Nicole A. Massoll
Keyword(s):  
Smooth Muscle ◽  
Case Report ◽  
Benign Tumor ◽  
Broad Ligament ◽  
Total Abdominal Hysterectomy ◽  
Abdominal Hysterectomy ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Hormonal Stimulation ◽  
Pelvic Organs

Abstract Adenomyoma is a benign tumor composed of smooth muscle and benign endometrium. These tumors typically originate within the uterus. An extrauterine adenomyoma is a rare entity. We report a uterine-like mass consistent with an extrauterine adenomyoma presenting 22 years following a total abdominal hysterectomy and bilateral salpingo-oophorectomy. The mass was pear-shaped with uterine-type smooth muscle and a cavity lined by functional endometrial glands and stroma. To our knowledge, only 4 other cases of an extrauterine uterine-like mass are reported in the literature. Three involved the ovary, while one was located adjacent to the broad ligament with normal pelvic organs. Although none of these other uterus-like masses were described as adenomyomas with uterine-like features, the histologic findings are strikingly similar. An understanding of the müllerian system suggests that either an embryologic malformation or a differential multipotentiality existing in the subcoelomic tissues in response to hormonal stimulation results in a supernumerary müllerian structure like a uterus, as observed in this case. The presence of endometrial glands and stroma in the mass confirms that the tissues in this mass are hormonally responsive. It is most likely that this uterine-like mass arose from the tissues of the secondary müllerian system in response to estrogenic stimulation.

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