Evidence map›Paper›PMID 33093769›Full record

SynthesisSarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG2020

Miliary Sarcoidosis: does it exist? A case series and systematic review of literature.

Srinivas Rajagopala, Sakthi Sankari, Roopa Kancherla, Ramanathan Palaniappan Ramanathan, Devanand Balalakshmoji

Open access · greenAbstract readCase ReportsSystematic Review
In one paragraph

Synthesis in Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Miliary sarcoidosis.Respirology case reports · 2024
    Article
  3. Imaging of Pulmonary Sarcoidosis-A Review.Journal of clinical medicine · 2024
    Review
  4. Article
  5. Article
  6. Pulmonary Sarcoidosis: Diagnosis and Differential Diagnosis.Diagnostics (Basel, Switzerland) · 2021
    Review
  7. Review
  8. Sarcoidosis: a prospective observational cohort from Northern Alberta.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2020
    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

5 authors at 1 institution in 1 country.

Srinivas RajagopalaDepartment of Pulmonary Medicine.
Sakthi SankariDepartment of Pathology and.
Roopa KancherlaDepartment of Pulmonary Medicine.
Ramanathan Palaniappan RamanathanDepartment of Pulmonary Medicine.
Devanand BalalakshmojiRadiodiagnosis, PSG Institute of Medical Sciences and Research, Peelamedu, Coimbatore, India.
PSG Institute of Medical Sciences & Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesSarcoidosis typically presents with peribronchovascular and perilymphatic nodules on high-resolution computed tomography (HRCT); a miliary pattern is reported but not well described. DESIGN

settingWe describe four patients with miliary sarcoidosis and results of a systematic review of all previously reported cases from 1985 onwards.

resultsWe identified only 27 cases of "miliary" sarcoidosis in the HRCT era. These patients were older (85.2% older than 40 years), had more co-morbidities (72.7%) and were symptomatic compared to "typical" sarcoidosis. Respiratory symptoms were present in 61.9% at diagnosis. Hypercalcemia was seen in 28.5%. On review of HRCT images, only 34.6% (9/26) had a "true miliary" pattern without fissural nodules. In our series, prominent perivascular granulomas were seen on histopathology in all. 44.4% (12/27) had tuberculosis preceding or concurrent to miliary sarcoidosis. Of the eight true associations, tuberculosis preceded sarcoidosis by 52 (median, IQR 36) weeks in six and occurred concurrently in another two. The diagnosis of tuberculosis was clinical in all with concurrent diagnosis of tuberculosis and sarcoidosis. Treatment with steroids had 100% response and 14.2% relapse.

conclusionsA true miliary pattern in the HRCT era is very rare in sarcoidosis and subtle perilymphatic pattern is nearly always seen; this should be labeled "pseudo-miliary". Prominent perivascular granulomas are associated with true miliary pattern. Miliary sarcoidosis patients are older and symptomatic, needing treatment at diagnosis. "Miliary" sarcoidosis may follow treatment for tuberculosis; concurrent cases possibly indicate the difficulty in differentiating both or a "tuberculo-sarcoid" presentation.

Indexed as

Tomography, X-Ray ComputedAdultAgedAntitubercular AgentsBacteriological TechniquesBiopsyDiagnosis, DifferentialFemaleHumansLungMaleMiddle AgedPredictive Value of TestsRecovery of FunctionRecurrenceSarcoidosis, PulmonaryAntitubercular AgentsSteroidsmicronodulesmiliarymiliary tuberculosissarcoidosis

Identifiers

PMID33093769
PMCPMC7569537
OpenAlexW3094363417

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.