Evidence map›Paper›PMID 42857398›Full record

ArticleInternational journal of surgery case reports2026

Gestational gigantomastia in the early postpartum period presenting with severe refractory pain: a case report.

Eskinder Amare Assefa, Tesfaye Aga Dinagde, Lukman Yusuf, Yonas Girma Shumiye, Eskindir Molla Nuru

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Article in International journal of surgery case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Eskinder Amare AssefaDepartment of Surgery, Yehuleshet Medical and Surgical Center, Addis Ababa, Ethiopia.ORCID https://orcid.org/0000-0001-9851-9633
Tesfaye Aga DinagdeDepartment of Surgery, Yehuleshet Medical and Surgical Center, Addis Ababa, Ethiopia.
Lukman YusufDepartment of Surgery, Yehuleshet Medical and Surgical Center, Addis Ababa, Ethiopia.
Yonas Girma ShumiyeDepartment of Surgery, Yehuleshet Medical and Surgical Center, Addis Ababa, Ethiopia.
Eskindir Molla NuruDepartment of Surgery, Ras Desta Damtew Memorial Hospital, Addis Ababa, Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Gestational gigantomastia (GG) is a rare, benign breast disorder characterized by rapid, excessive, and disproportionate breast enlargement during pregnancy. Affected patients may develop severe breast pain, skin breakdown, secondary infection, and musculoskeletal complications, resulting in significant functional impairment and psychosocial distress. Case presentation: We report the case of a 24-year-old woman (G2P1A1) who presented on the second postpartum day with a 5-month history of rapidly progressive bilateral breast enlargement and severe, disabling breast pain of 2 days' duration. Despite treatment with bromocriptine and multimodal analgesia, her pain remained refractory, necessitating emergent bilateral simple mastectomy. Histopathological examination confirmed GG, and the patient had an uneventful postoperative recovery. Discussion: GG is an uncommon clinical entity, with an estimated incidence ranging from 1 in 28 000 to 1 in 100 000 pregnancies. Although hormonal hypersensitivity is presumed to play a role, its etiology remains poorly understood. Medical management is generally recommended as first-line therapy; however, complete regression is uncommon, and the clinical response is often limited. Consequently, surgical management remains the definitive treatment option in many cases, particularly when complications arise or conservative therapy fails. Conclusion: Early postpartum GG with severe refractory pain requiring emergent bilateral mastectomy is exceedingly rare. Bilateral mastectomy with planned reconstruction may be an appropriate definitive treatment option when conservative measures fail, particularly for patients wishing to reduce the risk of recurrence during future pregnancies. Furthermore, this approach avoids the potential risk of life-threatening hemorrhage associated with the alternative surgical option of reduction mammoplasty.

Indexed as

benign breast disordersbilateral mastectomycase reportgestational gigantomastiagigantomastia

Identifiers

PMID42857398
PMCPMC13652467

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