Evidence map›Paper›PMID 29747617›Full record

ReviewBMC endocrine disorders2018

Pheochromocytoma as a rare cause of hypertension in a 46 X, i(X)(q10) turner syndrome: a case report and literature review.

Ji Yeon Shin, Bo Hyun Kim, Young Keum Kim, Tae Hwa Kim, Eun Heui Kim, Min Jin Lee, Jong Ho Kim, Yun Kyung Jeon, Sang Soo Kim, In Joo Kim

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in BMC endocrine disorders, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Ji Yeon ShinDepartment of Internal Medicine, Pusan National University College of Medicine, Busan, 49241, South Korea.
Bo Hyun KimDepartment of Internal Medicine, Pusan National University College of Medicine, Busan, 49241, South Korea. pons71@hanmail.net.ORCID http://orcid.org/0000-0001-9632-9457
Young Keum KimDepartment of Pathology, Pusan National University Hospital and Pusan National University School of Medicine, Busan, 49241, South Korea.
Tae Hwa KimDepartment of Internal Medicine, Pusan National University College of Medicine, Busan, 49241, South Korea.
Eun Heui KimDepartment of Internal Medicine, Pusan National University College of Medicine, Busan, 49241, South Korea.
Min Jin LeeDepartment of Internal Medicine, Pusan National University College of Medicine, Busan, 49241, South Korea.
Jong Ho KimDepartment of Internal Medicine, Pusan National University College of Medicine, Busan, 49241, South Korea.
Yun Kyung JeonDepartment of Internal Medicine, Pusan National University College of Medicine, Busan, 49241, South Korea.
Sang Soo KimDepartment of Internal Medicine, Pusan National University College of Medicine, Busan, 49241, South Korea.
In Joo KimDepartment of Internal Medicine, Pusan National University College of Medicine, Busan, 49241, South Korea.
Pusan National University · KRPusan National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiovascular disease (CVD) presents the most serious health problems and contributes to the increased mortality in young women with Turner syndrome. Arterial hypertension in Turner syndrome patients is significantly more prevalent than that in a general age-matched control group. The aetiology of hypertension in Turner syndrome varies, even in the absence of cardiac anomalies and obvious structural renal abnormalities. Pheochromocytoma is an extremely rare cause among various etiologies for hypertension in patients with Turner syndrome. Here, we reported a pheochromocytoma as a rare cause of hypertension in Turner syndrome patient. CASE PRESENTATION: A 21-year-old woman who has diagnosed with Turner syndrome with a karyotype of 46,X,i(X)(q10) visited for hypertension and mild headache. Transthoracic echography (TTE) showed no definite persistent ductus arteriosus shunt flow and cardiac valve abnormalities. Considering other important secondary causes like pheochromocytoma, hormonal studies were performed and the results showed increased serum norepinephrine, serum normetanephrine, and 24 h urine norepinephrine. We performed an abdominal computed tomography (CT) to confirm the location of pheochromocytoma. Abdominal CT showed a 1.9 cm right adrenal mass. I-131 meta-iodobenzylguanidine (MIBG) scintigraphy showed a right adrenal uptake. Laparoscopic adrenalectomy was performed and confirmed a pheochromocytoma. After surgery, blood pressure was within normal ranges and postoperative course was uneventful, and no recurrence developed via biochemical tests and abdominal CT until 24 months.

conclusionOur case and previous literatures suggest that hypertension caused by pheochromocytoma which is a rare but important and potentially lethal cause of hypertension in Turner syndrome. This case underlines the importance of early detection of pheochromocytoma in Turner syndrome. Clinicians should keep in mind that pheochromocytoma can be a cause of hypertension in patients with Turner syndrome.

Indexed as

Chromosome AberrationsChromosomes, Human, XAdrenal Gland NeoplasmsAdultFemaleHumansHypertensionPheochromocytomaPrognosisTurner SyndromeYoung AdultHypertensionPheochromocytomaTurner syndrome

Identifiers

PMID29747617
PMCPMC5946487
OpenAlexW2806328611

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.