Evidence map›Paper›PMID 27440277›Full record

ReviewThe American journal of case reports2016

Intestinal Lymphangiectasia: Insights on Management and Literature Review.

Mohamad J Alshikho, Joud M Talas, Salem I Noureldine, Saf Zazou, Aladdin Addas, Haitham Kurabi, Mahmoud Nasser

Open access · hybridAbstract readCase ReportsReview
In one paragraph

Review in The American journal of case reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Article
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  7. Article
  8. Article
  9. Review
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  13. Intralesional bleomycin injection treatment of intra-abdominal lymphangiomas presenting with acute abdomen in children.Ulusal travma ve acil cerrahi dergisi = Turkish journal of trauma & emergency surgery : TJTES · 2023
    Article
  14. Review
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  18. Review
  19. Article
  20. Pediatric localized intestinal lymphangiectasia treated with resection.International medical case reports journal · 2019
    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

7 authors at 3 institutions in 2 countries.

Mohamad J AlshikhoDepartment of Neurology, Massachusetts General Hospital, Harvard University, Boston, MA, USA.
Joud M TalasDepartment of Dermatology, Aleppo University, Aleppo, Syrian Arab Republic.
Salem I NoureldineDepartment of Otolaryngology - Head and Neck Surgery, Johns Hopkins University, Baltimore, MD, USA.
Saf ZazouDepartment of General Internal Medicine, Aleppo University, Aleppo, Syrian Arab Republic.
Aladdin AddasDepartment of General Internal Medicine, Aleppo University, Aleppo, Syrian Arab Republic.
Haitham KurabiDepartment of General Internal Medicine, Aleppo University, Aleppo, Syrian Arab Republic.
Mahmoud NasserDepartment of Gastroenterology, Aleppo University, Aleppo, Syrian Arab Republic.
University of Aleppo · SYHarvard University · USJohns Hopkins University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Intestinal lymphangiectasia (IL) is a rare disease characterized by a dilatation of the intestinal lymphatics and loss of lymph fluid into the gastrointestinal tract leading to hypoproteinemia, edema, lymphocytopenia, hypogammaglobinemia, and immunological abnormalities. Iron, calcium, and other serum components (e.g., lipids, fat soluble vitamins) may also be depleted. A literature search revealed more than 200 reported cases of IL. Herein, we report our observations of a patient diagnosed with IL; we also present our conclusion for our review of the published literature. CASE REPORT A 24-year-old male was admitted to Aleppo University Hospital with the complaints of abdominal pain, headache, arthralgia, fever, and rigors. His past medical history was remarkable for frequent episodes of diarrhea, recurrent infections, and swelling in the lower limbs. In addition, he had been hospitalized several times in non-academic hospitals due to edema in his legs, cellulitis, and recurrent infections. In the emergency department, a physical examination revealed a patient in distress. He was weak, dehydrated, pale, and had a high-grade fever. His lower extremities were edematous, swollen, and extremely tender to touch. The overlying skin was erythematous and warm. Moreover, the patient was tachycardic, tacypneic, and moderately hypotensive. The patient was resuscitated with IV fluids, and Tylenol was administered to bring the temperature down. Blood tests showed anemia and high levels of inflammatory markers. The patient's white blood cell count was elevated with an obvious left shift. However, subsequent investigations showed that the patient had IL. Suitable diet modification plans were applied as a long-term management plan. CONCLUSIONS IL is a rare disease of challenging nature due to its systematic effects and lack of comprehensive studies that can evaluate the effectiveness of specific treatments in a large cohort of patients. MCT (medium-chain triglyceride) oils and diet modification strategies are effective in reducing the loss of body proteins and in maintaining near-normal blood levels of immunoglobulins. However, octreotide and MCT oils had no proven role in shrinking edema in our patient.

Indexed as

Disease ManagementBiopsyDiagnosis, DifferentialDiarrheaEndoscopy, Digestive SystemHumansIntestinesLymphangiectasis, IntestinalMaleRadiography, AbdominalTomography, X-Ray ComputedUltrasonographyYoung Adult

Identifiers

PMID27440277
PMCPMC4957630
OpenAlexW2493230398

What OpenQuestion holds

Textmetadata
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.