# From post-war reconstruction to the twenty-first century – ophthalmic pathology in Freiburg 1945–2015. Part 2: review of 43,169 histological diagnoses from 39,256 specimens collected over 71 years at a large German tertiary eye care centre

**Authors:** Simone Nuessle, Mateusz Glegola, Tabea Schulz, Thomas Reinhard, Johannes Haedrich, Claudia Auw-Haedrich

PMC · DOI: 10.1186/s12886-025-04522-w · BMC Ophthalmology · 2026-01-16

## TL;DR

This study analyzes 71 years of eye disease diagnoses in Freiburg, showing how trends in conditions like chalazion and pterygium have changed over time due to medical advances and environmental factors.

## Contribution

The paper provides a comprehensive, long-term analysis of ophthalmic pathology trends using a large dataset from a single tertiary center over 71 years.

## Key findings

- The eyelid was the most common site of diagnosis, with chalazion, basal cell carcinoma, and papilloma being the top conditions.
- There was an increase in chalazion, Fuchs’ dystrophy, and pterygium, linked to surgical advancements and UV exposure.
- A decline in squamous cell carcinoma and younger age at basal cell carcinoma diagnosis suggests improved UV protection and earlier detection.

## Abstract

Ophthalmic pathology is essential for diagnosing ocular diseases, correlating clinical and histopathological findings, and advancing research. The Eye Center at the University of Freiburg, Germany, has archived histopathological specimens since 1945, offering a unique resource to analyse long-term diagnostic trends. This study examines 43,169 diagnoses from 39,256 specimens over 71 years (1945–2015), providing insights into the evolution of ophthalmic pathology at a major tertiary care centre.

We performed a retrospective analysis of all archived ophthalmic pathology reports, categorising specimens by anatomical region and recording diagnoses, patient age and surgery dates. Data were analysed mostly in 10-year intervals, with annual sub-analyses for the four most frequent sites. Statistical parameters assessed changes in diagnostic frequency, patient demographics, and age-related trends. Results were compared with 38 international studies to contextualise findings.

The eyelid was the most common site (50%), with chalazion (18%), basal cell carcinoma (BCC) (16%), and papilloma (16%) as the leading diagnoses. The cornea (17%) was dominated by Fuchs’ dystrophy (19%), keratoconus (13%), and keratitis (11%), while pterygium (29%) and nevus (12%) prevailed in the conjunctiva (14%). In the orbit (1.2%), inflammation (12%) and lymphoma (9.5%) were most frequent. Key trends included a rise in chalazion, Fuchs’ dystrophy, and pterygium, linked to surgical advancements (e.g. microsurgery, DMEK) and increased UV exposure. The age range of patients widened for most diagnoses, reflecting an aging population and broader surgical indications. A decline in squamous cell carcinoma (SCC) and younger age at BCC diagnosis suggest improved UV protection and earlier detection. Regional comparisons revealed higher rates of chalazion and BCC in Freiburg than in Asian cohorts, likely due to genetic and environmental factors.

This 71-year analysis highlights dynamic shifts in ophthalmic pathology, shaped by historical events, clinical progress, demographics, and environmental influences. The study emphasises the vital role of ophthalmologists in pathology, ensuring integrated clinical-histopathological expertise for accurate diagnoses and optimal patient outcomes. Our study data offer valuable insights into the frequency and evolving trends of the most common diagnoses over an extended period. These findings support future research in molecular diagnostics and global comparative studies, reinforcing the importance of ophthalmologist-led ophthalmic pathology in specialised eye care.

## Linked entities

- **Diseases:** chalazion (MONDO:0005844), basal cell carcinoma (MONDO:0005341), papilloma (MONDO:0002363), keratoconus (MONDO:0015486), keratitis (MONDO:0003085), pterygium (MONDO:0005085), nevus (MONDO:0005073), lymphoma (MONDO:0003659), squamous cell carcinoma (MONDO:0005096)

## Full-text entities

- **Genes:** BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, PVR (PVR cell adhesion molecule) [NCBI Gene 5817] {aka CD155, HVED, NECL5, Necl-5, PVS, TAGE4}
- **Diseases:** Dermoid cysts (MESH:D003884), muscular dystrophy (MESH:D009136), Ulcerative and infectious keratitis (MESH:D003320), lacrimal gland pleomorphic adenomas (MESH:C563250), prolapse (MESH:D011391), PHPV (MESH:D054514), poorly differentiated (MESH:D020522), inflammatory eye conditions (MESH:D005128), BCC (MESH:D002280), hemangioma (MESH:D006391), herpes zoster keratitis (MESH:D006562), Cornea (MESH:D065306), Fuchs' dystrophy (MESH:D005642), Philadelphia (MESH:D010677), CNV (MESH:D002833), eyelid lesions (MESH:D005141), cysts (MESH:D003560), chronic disease (MESH:D002908), MG (MESH:D009157), bacterial infections (MESH:D001424), foreign (MESH:D005547), Lymphoma (MESH:D008223), EOPS (MESH:C000719191), foreign body granuloma (MESH:D015745), Descemet's membrane (MESH:D015433), cataracts (MESH:D002386), Salzmann nodular degeneration (MESH:D009410), Dacryocystitis (MESH:D003607), Papillomas (MESH:D010212), breast and lung cancers (MESH:D001943), inflammatory and lymphoproliferative lesions (MESH:D008232), B-cell lymphoma (MESH:D016393), Orbital pseudotumour (MESH:D009916), postoperative (MESH:D019106), glaucoma (MESH:D005901), Perforating keratoplasty (MESH:D057112), pathologies (MESH:D005598), retinal pathologies (MESH:D012164), tuberculosis infection (MESH:D014376), Granuloma (MESH:D006099), Pleomorphic adenoma (MESH:D008949), normal iris and iris melanoma (MESH:D007499), Meibomian gland carcinoma (MESH:D000080343), NHL (MESH:D008228), corneal infection (MESH:D007239), Nevi (MESH:D009506), TS (MESH:D005879), dystrophies (MESH:D058499), lymphangiomas (MESH:D008202), corneal dystrophies (MESH:D003317), Primary (MESH:D010538), hypertrophy (MESH:D006984), Conjunctiva (MESH:C563620), sarcoidosis (MESH:D012507), Herpes simplex (MESH:D006561), dry eye (MESH:D015352), EMZL (MESH:D018442), bacterial endophthalmitis (MESH:D009877), pinguecula (MESH:D059407), ulcerative (MESH:D014456)
- **Chemicals:** steroids (MESH:D013256), melanin (MESH:D008543), BK (-), vismodegib (MESH:C538724)
- **Species:** Homo sapiens (human, species) [taxon 9606], Kayvirus kay (species) [taxon 221915]

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12809991/full.md

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Source: https://tomesphere.com/paper/PMC12809991