Evidence map›Paper›PMID 34932395›Full record

ReviewThe Journal of international medical research2021

Not the final diagnosis: from Addison's disease to POEMS syndrome: a case report and literature review.

Xiaoxi Xie, Rao Li, Yongxia Lu, Xuan Li, Pu Kuang, Chunhui Wang, Nanwei Tong, Qingguo Lü

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in The Journal of international medical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 3 institutions in 2 countries.

Xiaoxi XieDepartment of Gastroenterology, West China Hospital of Sichuan University, Chengdu, China.ORCID https://orcid.org/0000-0001-5538-4345
Rao LiDepartment of Endocrinology and Metabolism, West China Hospital of Sichuan University/West China School of Nursing, Sichuan University, Chengdu, China.
Yongxia LuDepartment of Endocrinology and Metabolism, Chengdu Seventh People's Hospital, Chengdu, China.
Xuan LiDepartment of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, MS, USA.
Pu KuangDepartment of Haematology, West China Hospital of Sichuan University, Chengdu, China.
Chunhui WangDepartment of Gastroenterology, West China Hospital of Sichuan University, Chengdu, China.
Nanwei TongDepartment of Endocrinology and Metabolism, West China Hospital of Sichuan University, Chengdu, China.
Qingguo LüDepartment of Endocrinology and Metabolism, West China Hospital of Sichuan University, Chengdu, China.
Sichuan University · CNJackson Memorial Hospital · USSeventh People's Hospital of Shanghai · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the case of a 47-year-old male patient with pigmentation of the head, face and hands, who was initially diagnosed as having primary adrenal insufficiency (Addison's disease). Laboratory testing, imaging and physical examination revealed subclinical hypothyroidism, high circulating prolactin and oestradiol concentrations, gynaecomastia, lymphadenopathy, splenomegaly and weakness of both lower limbs. These findings led us to consider whether a single or multiple diseases were present in this patient. Indeed, Addison's disease can represent one aspect of a wider systemic disease. Therefore, we performed further examinations, and found high serum M protein (5.1%) and vascular endothelial growth factor [1005.30 pg/mL (normal range 0 to 142 pg/mL)] concentrations. As a consequence, we diagnosed polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes (POEMS) syndrome. Consequently, when a single disease cannot fully explain the multiple symptoms and signs of one patient, clinicians should consider the possibility of the presence of a wider syndrome and undertake more detailed diagnostic testing.

Indexed as

Addison DiseasePOEMS SyndromeHumansMaleMiddle AgedSplenomegalyVascular Endothelial Growth Factor AVascular Endothelial Growth Factor AAddison’s diseaseendocrinopathyhypothyroidismmonoclonal gammopathy and skin changes syndromeM proteinorganomegalyPolyneuropathyskin pigmentationvascular endothelial growth factor

Identifiers

PMID34932395
PMCPMC8826110
OpenAlexW4200259257

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.