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Sterile pustules in dermatology
Corresponding author: Dr. Harshini Penala, Department of Dermatology, Venereology and Leprosy, Raja Venkata Boina Institute of Medical Sciences and Research Center, Hanamkonda, Telangana, India. harshini0120@gmail.com
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Received: ,
Accepted: ,
How to cite this article: Penala H, Bhagyashree M, Matety AR. Sterile pustules in dermatology. Indian J Dermatol Venereol Leprol. doi: 10.25259/IJDVL_383_2025
Sterile pustules are pus-filled lesions that yield no bacteria, fungi, or viruses on culture. They serve as key diagnostic clues in a range of dermatological conditions, from benign to life-threatening. Accurate recognition is essential for dermatology residents, as management depends on the underlying cause.
Classification
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1)
Infantile
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2)
Glandular
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3)
Autoimmune
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4)
Neutrophilic dermatoses
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5)
Iatrogenic
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6)
Insect bite reactions
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7)
Miscellaneous
Infantile
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1.
Erythema toxicum neonatorum (ETN): It is common in 75% of term newborns. It is seen within 24-48 hours after birth. It appears as blotchy erythematous macules with central pustules.
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2.
Transient neonatal pustular melanosis (TNPM): It is seen at birth or within 3 weeks. It features superficial pustules healing with hyperpigmented macules and collarettes of scale.
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3.
Infantile acropustulosis: It presents as recurrent, pruritic pustules on palms and soles in infants.
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4.
Eosinophilic pustular folliculitis of infancy: It presents as annular clusters of follicular pustules on the scalp with associated eosinophilia.1
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5.
Glandular miliaria pustulosa: It shows intraepidermal sterile pustules due to sweat duct obstruction. It is a pustular form of miliaria.2
Autoimmune
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1.
Pustular psoriasis: It features sterile pustules; the condition may be localised (palmoplantar, acrodermatitis continua) or generalised (Von Zumbusch, pregnancy-related) [Figure 1].
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2.
Relapsing polychondritis: It includes auricular inflammation and sterile pustules.
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3.
IgA pemphigus: It presents as pustules in intertriginous areas with IgA deposition.
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4.
Early pemphigus foliaceus: It may present as subcorneal sterile pustules with biopsy showing acantholysis.
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5.
SAPHO syndrome: It’s features include sterile palmoplantar pustules, osteitis, and synovitis.

- Numerous pin-point discrete pustules on an erythematous base with few areas of desquamation on posterior trunk in a case of pustular psoriasis.
Neutrophilic dermatosis
1. Pyoderma gangrenosum
It causes chronic, recurrent, sterile pustular ulcers associated with inflammatory bowel disease. The pustular variant features discrete pustules surrounded by a halo, mainly on the lower limbs, trunk, and mucosa.
2. Sweet syndrome
Also known as acute febrile neutrophilic dermatosis, it presents with fever, erythematous plaques and raised neutrophil count. The pustular variant is rarer and linked to inflammatory bowel disease.
3. Behcet disease
It presents with recurrent oral and genital aphthae, pseudo-folliculitis with sterile pustules, erythema nodosum, and acneiform eruptions.
4. Subcorneal pustular dermatosis (Sneddon-Wilkinson Disease)
It causes sterile, flaccid pustules often in flexural areas. The hypopyon sign is characteristic [Figure 2].

- A single pustule with the characteristic hypopyon signin subcorneal pustular dermatoses.
6. Neutrophilic eccrine hidradenitis
It is seen commonly in patients receiving chemotherapy; presents as tender erythematous plaques studded with sterile pustules, often involving eccrine-rich areas.
Iatrogenic
1. Acute generalised exanthematous pustulosis (AGEP)
AGEP is a severe drug reaction that typically manifests with the rapid development of multiple, non-follicular, sterile, pinhead-sized pustules that usually occur a few hours to a few days after exposure to an offending drug, most often an antibiotic (eg, aminopenicillins, quinolones, pristinamycin, etc.) [Figure 3].

- Multiple, discrete, pinpoint pustules on an erythematous base on upper back seen in a patient after taking tablet amoxicillin.
2. Bowel-associated dermatitis-arthritis syndrome (BADAS)
BADAS is characterised by presence of sterile pustular vasculitis associated with blind loops of bowel or other causes of stasis of bowel contents. It is usually seen following jejunoileal bypass or gastric resection.2
3. Drug-induced
Prolonged intake of drugs like topical and systemic corticosteroids, along with certain other drugs [Table 1]1 can result in pustular lesions with other cutaneous manifestations [Figure 4].
| Drug class | Examples |
|---|---|
| Antibiotics | Beta-lactams (amoxicillin, ceftriaxone), macrolides, fluoroquinolones, sulfonamides |
| Antifungals | Terbinafine, griseofulvin |
| Antimalarials | Hydroxychloroquine, chloroquine |
| Antiepileptics | Carbamazepine, phenytoin, lamotrigine |
| NSAIDs | Ibuprofen, naproxen, diclofenac |
| CCBs | Diltiazem, amlodipine |
| Anti-hypertensives | ACE inhibitors (enalapril, lisinopril) |
| Allopurinol | Frequently implicated in AGEP |
| Biologics | TNF-alpha inhibitors (infliximab, etanercept) |
| Immune checkpoint inhibitors | Nivolumab, pembrolizumab |
| EGFR inhibitors | Erlotinib, gefitinib, cetuximab |
| Corticosteroids | Systemic and topical misuse or withdrawal |
| Lithium | Often triggers pustular and acneiform eruptions |
| Vaccines | COVID-19, influenza (rare cases reported) |
NSAIDs: Non-steroidal anti-inflammatory drugs, CCBs: Calcium channel blockers, ACE: Angiotensin converting enzyme inhibitors, AGEP: Acute generalised exanthematous pustulosis, TNF: Tumour necrosis factor.

- Numerous papules and pustules with crusting and serous discharge on face after application of topical betamethasone for 6 months.
PRIDE COMPLEX: Papulopustulas and/or paronychia, regulatory abnormalities of hair growth, itching, and dryness due to Epidermal growth factor receptors (EGFR) inhibitors1 [Figure 5].

- Multiple papules and pustules on eyebrows after taking tablet erlotinib for lung carcinoma.
4. Post-photodynamic therapy (PDT)
Topical photodynamic therapy has been used for a diverse range of conditions in dermatology. Acute and short-term effects of PDT are itch, pain, oedema, crusting, sterile pustules, infection, erosive pustular dermatosis, and bullous pemphigoid.3
Insect bite reactions
Certain insect bite reactions like Hymenoptera and fire ants are characterised by pleomorphic lesions like urticarial papules, nodules, vesiculobullous lesions, and sterile pustules.
Miscellaneous
1. Eosinophilic pustular folliculitis
Three clinical types have been described as follows:
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a)
Classic eosinophilic pustular folliculitis (Ofuji disease) – It is most common in the Japanese population, characterised by chronic, recurrent follicular sterile pustules that tend to form a circinate pattern.
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b)
Eosinophilic folliculitis of immunosuppression- It is most common in patients with HIV, characterised by papules and sterile pustules involving the face and upper trunk.
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c)
Eosinophilic pustular folliculitis of infancy. It presents as annular clusters of follicular pustules on the scalp with associated eosinophilia.
2. Irritant contact dermatitis (ICD)
Irritant contact dermatitis is the cutaneous response to the physical or toxic effects of a wide range of environmental exposures. This may be an acute irritant contact dermatitis or a cumulative irritant dermatitis. ICD has a spectrum of clinical features, ranging from a little dryness to various types of eczematous dermatitis. The pustules, which as a part of this spectrum are usually sterile unless secondarily infected1 [Figure 6a and 6b].

- Numerous pinhead sized papules and pustules in peri-nasal and peri-oral areas in a patient after playing with holi colours.

- ICD-Close up view. (ICD: Irritant contact dermatitis).
3. Erosive pustular dermatosis
It classically presents as sterile pustules, keratotic crusts, erosions, and mild inflammation arising within the atrophic, photodamaged skin of a bald scalp. It is one of the cutaneous manifestations of chronically photodamaged skin.4
4. Acute generalised pustular bacterid
It is a rare dermatosis presenting as sterile pustules on an erythematous base, commonly involving palms and soles, thought to be a reaction to an infectious focus elsewhere.5 These conditions must also be carefully differentiated from clinically similar infective pustular dermatoses. A list of commonly encountered sterile pustular conditions is provided in Table 21, while Table 31 offers an overview to aid in clinical evaluation and decision-making. Table 4 offers the overview of sterile pustules in dermatology.
| Infective condition | Distinguishing features |
|---|---|
| Bacterial folliculitis | Folliculocentric pustules with erythematous halos; Staphylococcus aureus is usually cultured from pustular fluid. |
| Cutaneous candidiasis | Pustules with surrounding erythema in intertriginous zones; satellite pustules are typical; KOH mount shows budding yeast and pseudohyphae. |
| Tinea corporis (pustular type) | Annular scaly plaques with peripheral pustules; KOH mount shows septate hyphae. |
| Viral pustulosis (HSV, VZV) | Grouped vesiculo-pustules, often with burning or pain; Tzanck smear shows multinucleated giant cells. |
| Impetigo (bullous and non-bullous) | Honey-coloured crusts over pustules, especially around the mouth and nose; Gram stain shows gram-positive cocci. |
| Secondary syphilis (pustular variant) | Pustular syphilids on palms and soles; serological tests (VDRL, TPHA) confirm diagnosis. |
| Pustular ecthyma gangrenosum | Necrotic pustules in immunocompromised patients; cultures reveal Pseudomonas aeruginosa. |
| Dermatophytid reaction (id reaction) | Pustular lesions distant from primary dermatophyte infection; the primary site shows fungal elements on KOH, secondary pustules are sterile. |
KOH: Potassium hydroxide mount, HSV: Herpes simplex virus, VZV: Varicella zoster virus, TPHA: Treponela pallidum hemagglutination assay.
| Condition | First line treatment |
|---|---|
| 1. ETM, TNPM | Resolves spontaneously in 6-8 weeks |
| 2. Eosinophilic folliculitis of infancy | |
| 3. Infantile acropustulosis | Moderate-to-high potency topical corticosteroids are useful for treatment. |
| 4. Miliaria pustulosa | Management involves prevention of further sweating and skin cooling (fans, air conditioning) with oral vitamin C 500mg twice daily. |
| 5. Pustular psoriasis | Oral retinoids are the first-line treatment option and systemic steroids in case of pregnancy. |
| 6. Relapsing polychondritis | Corticosteroids, often prednisone. |
| 7. IgA pemphigus | Oral and topical corticosteroids, often with dapsone to reduce neutrophil infiltration. |
| 8. Early pemphigus foliaceus (PF) | Topical corticosteroids. |
| 9. SAPHO syndrome | Non-steroidal anti-inflammatory drugs (NSAIDs) for pain relief. |
| 10. Pyoderma gangrenosum (PG) | Systemic corticosteroids |
| 11. Sweet’s syndrome | Limited disease: topical and intralesional steroids; Extensive disease: systemic steroids. |
| 12. Behçet’s disease | Treatment for oral lesions: topical corticosteroids in orabase; Systemic disease: colchicine is first-line. |
| 13. Subcorneal pustular dermatosis | Dapsone |
| 14. Amicrobial pustulosis of the folds | Corticosteroids, often prednisone. |
| 15. Neutrophilic eccrine hidradenitis | Corticosteroids, often prednisone. |
| 16. AGEP | Stop the offending drug with supportive care. |
| 17. BADAS | Combination of oral antibiotics and corticosteroids. |
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18. Drug-induced 19. Post-photodynamic therapy |
Lesions resolve spontaneously after stopping the offending agent. |
| 20. Insect bite reactions | Treatment is based on severity either topical or systemic steroids. |
|
21. Eosinophilic pustular folliculitis 22. Irritant contact dermatitis (ICD) 23. Erosive pustular dermatosis |
Treatment is based on severity; topical or oral steroids can be given. |
| 24. Acute generalised pustular bacterid | Treating the infectious foci will cause resolution of these lesions. |
| 25. Sterile folliculitis from occlusion | Avoid occlusion. |
ETN: Erythema toxicum neonatorum, TNPM: Total neonatal pustular melanosis, SAPHO: Synovitis, acne, pustulosis, hyperosteosis, osteitis
| Infantile | Glandular | Autoimmune | Neutrophilic | Iatrogenic | Insect bite rections | Miscellaneous |
|---|---|---|---|---|---|---|
| • Erythema toxicum neonatorum | • Miliaria pustulosa | • Pustular psoriasis-Palmoplantar pustulosis, Acrodermatitis continua of Hallopeau, Pustular psoriasis of pregnancy. |
• Pyoderma gangrenosum |
• Acute generalised exanthematous pustulosis (AGEP) |
• Hymenoptera sting. |
• Eosinophilic pustular folliculitis- |
| • Transient neonatal pustular melanosis |
• AGEP |
• Sweet syndrome | • Bowel-associated dermatitis-arthritis syndrome (BADAS) | • Fire ants sting. | • Classic eosinophilic pustular folliculitis (Ofuji disease), | |
| • Eosinophilic pustular folliculitis of infancy | • Relapsing polychondritis | • Behçet’s syndrome | • Drug induced | • Eosinophilic pustular folliculitis associated with immunosuppression | ||
| • SAPHO syndrome | • Subcorneal pustular dermatoses (SCPD) | . Topical and systemic corticosteroids, | • Eosinophilic pustular folliculitis of infancy. | |||
| • Amicrobial pustulosis of folds. |
PRIDE complex: EGFR-inhibitors • Post-hair transplantation folliculitis • Post-photodynamic therapy |
• Irritant contact dermatitis. | ||||
| • Erosive pustular dermatosis. |
EGFR: Epidermal growth factor receptor
Conclusion
Sterile pustules span a wide dermatological spectrum, ranging from benign, self-limited conditions seen in neonates to chronic, relapsing autoimmune or neutrophilic dermatoses. A systematic approach, considering clinical presentation, age of onset, distribution, systemic associations, and histopathological features, is crucial for accurate diagnosis and effective management.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent.
Financial support and sponsorship
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Conflicts of interest
There are no conflicts of interest.
Use of artificial intelligence (AI)-assisted technology for manuscript preparation
The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.
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