Clues in Histopathological Diagnosis of Panniculitis

Background: Panniculitides comprise a group of heterogeneous inflammatory diseases. Nevertheless, histopathological study along with clinicopathological correlation usually led to a specific diagnosis. In most textbooks, the first step in the diagnosis is to classify them as mostly septal or lobular depending on where the inflammatory infiltrate is located. The second step is deciding if vasculitis is present or not. Finally, the third step is further characterizing the inflammatory infiltrate. However, in addition to the algorithmic approach to panniculitis diagnosis, some subtle changes may help to the diagnosis. Objective: To review some clues in panniculitis dermatopathological diagnosis such as presence of granulation tissue, sclerotic connective tissue septa, small granulomas arranged around a central clear space, so-called ghost adipocytes, needle-shaped crystals, small lobules with a proliferation of capillaries, Splendore-Hoeppli phenomenon, refractile microspheres, neutrophilic infiltrates, granulomas and fibroplasia or presence of adipose tissue in dermis. Methods: We have compiled 12 clues based in our personal experience in this field. Limitations: Specificity and sensibility of every clue may vary and these clues are a guide to correct diagnoses that should rely in clinicopathological correlation. Conclusion: Knowledge of these 12 clues will help to increase the diagnostic accuracy in panniculitis diagnosis.

[1]  N. Walsh,et al.  Postirradiation pseudosclerodermatous panniculitis with involvement of breast parenchyma: a dramatic example of a rare entity and a pitfall in diagnosis , 2016, Journal of cutaneous pathology.

[2]  Á. Santos-Briz,et al.  Exenatide-Induced Eosinophil-Rich Granulomatous Panniculitis: A Novel Case Showing Injected Microspheres. , 2015, The American Journal of dermatopathology.

[3]  M. Llamas-Velasco,et al.  Panniculitis with crystals induced by etanercept subcutaneous injection , 2015, Journal of cutaneous pathology.

[4]  G. Fraga,et al.  Splendore-Hoeppli reaction and muscular arteritis in pancreatic panniculitis. , 2015, Journal of cutaneous pathology.

[5]  S. Varothai,et al.  Disseminated gouty panniculitis: an unusual presentation of extensive cutaneous tophi , 2014, Dermatology practical & conceptual.

[6]  M. Chan Neutrophilic panniculitis: algorithmic approach to a heterogeneous group of disorders. , 2014, Archives of pathology & laboratory medicine.

[7]  Ying Guo,et al.  Exenatide-induced eosinophilic sclerosing lipogranuloma at the injection site. , 2014, The American Journal of dermatopathology.

[8]  M. Stone,et al.  Eosinophil‐rich granulomatous panniculitis caused by exenatide injection , 2014, Journal of cutaneous pathology.

[9]  Shilpa Kanathur,et al.  Post-steroid panniculitis: A rare case report , 2013, Indian dermatology online journal.

[10]  L. Requena,et al.  Postirradiation pseudosclerodermatous panniculitis: three new cases with additional histopathologic features supporting the radiotherapy etiology. , 2013, The American Journal of dermatopathology.

[11]  Hyun Su Park,et al.  Localized Involutional Lipoatrophy in a Child , 2013, Annals of dermatology.

[12]  A. Torrelo,et al.  Cutaneous aspergillosis mimicking pancreatic and gouty panniculitis. , 2012, Journal of the American Academy of Dermatology.

[13]  Á. Santos-Briz,et al.  Gemcitabine‐associated livedoid thrombotic microangiopathy with associated sclerema neonatorum‐like microscopic changes , 2012, Journal of cutaneous pathology.

[14]  Z. Argényi,et al.  Cutaneous and mucosal mucormycosis mimicking pancreatic panniculitis and gouty panniculitis. , 2012, Journal of the American Academy of Dermatology.

[15]  M. Llamas-Velasco,et al.  [Fibrosing cutaneous sarcoidosis]. , 2012, Actas dermo-sifiliograficas.

[16]  D. S. Santa Cruz,et al.  Lipodermatosclerosis: a clinicopathological study of 25 cases. , 2010, Journal of the American Academy of Dermatology.

[17]  Masaaki Ito,et al.  Tuberculoid granulomas in cutaneous sarcoidosis: a study of 49 cases , 2010, Journal of cutaneous pathology.

[18]  J. Bhawan,et al.  Sclerotic bodies in nephrogenic systemic fibrosis: a new histopathologic finding , 2009, Journal of cutaneous pathology.

[19]  Mahmoud R. Hussein,et al.  Mucocutaneous Splendore‐Hoeppli phenomenon , 2008, Journal of cutaneous pathology.

[20]  G. Guhl,et al.  Subcutaneous sweet syndrome. , 2008, Dermatologic clinics.

[21]  S. Segura,et al.  Anatomy and histology of normal subcutaneous fat, necrosis of adipocytes, and classification of the panniculitides. , 2008, Dermatologic clinics.

[22]  G. Darmstadt,et al.  Sclerema neonatorum: a review of nomenclature, clinical presentation, histological features, differential diagnoses and management , 2008, Journal of Perinatology.

[23]  F. Vanaclocha,et al.  Pancreatic panniculitis. , 2008, Dermatologic clinics.

[24]  J. Peyri,et al.  Traumatic panniculitis. , 2008, Dermatologic clinics.

[25]  P. Leboit,et al.  Pseudoxanthoma elasticum‐like fibers in the inflamed skin of patients without pseudoxanthoma elasticum , 2007, Journal of cutaneous pathology.

[26]  K. Resnik Subcutaneous sarcoidosis histopathologically manifested as fibrosing granulomatous panniculitis. , 2006, Journal of the American Academy of Dermatology.

[27]  S. Vernon,et al.  Cutaneous Zygomycosis Associated With Urate Panniculitis , 2006, American journal of dermatopathology.

[28]  J. Peyri,et al.  Subcutaneous sarcoidosis—clinicopathological study of 10 cases , 2005, The British journal of dermatology.

[29]  H. Walling,et al.  Alpha-1-antitrypsin associated panniculitis: the MS variant. , 2004, Journal of the American Academy of Dermatology.

[30]  K. Resnik The findings do not conform precisely: fibrosing sarcoidal expressions of panniculitis as example. , 2004, The American Journal of dermatopathology.

[31]  Philip R. Cohen,et al.  Sweet's syndrome revisited: a review of disease concepts , 2003, International journal of dermatology.

[32]  L. Robinson-Bostom,et al.  Alpha1-antitrypsin deficiency panniculitis. , 2003, Cutis.

[33]  Toshiyuki Yamamoto,et al.  Localized Involutional Lipoatrophy: Report of Six Cases , 2002, The Journal of dermatology.

[34]  R. Solans,et al.  Panniculitis: a cutaneous manifestation of dermatomyositis. , 2002, Journal of the American Academy of Dermatology.

[35]  L. Requena,et al.  Panniculitis. Part II. Mostly lobular panniculitis. , 2001, Journal of the American Academy of Dermatology.

[36]  L. Requena,et al.  Panniculitis. Part I. Mostly septal panniculitis. , 2001, Journal of the American Academy of Dermatology.

[37]  J. Toribio,et al.  Association of Sweet syndrome and erythema nodosum. , 2000, Archives of dermatology.

[38]  F. Tausk,et al.  T‐cell chronic lymphocytic leukemia mimicking dermatomyositis , 2000, International journal of dermatology.

[39]  W. White,et al.  Panniculitis: recent developments and observations. , 1996, Seminars in cutaneous medicine and surgery.

[40]  R. Winkelmann,et al.  Localized involutional lipoatrophy: a clinicopathologic study of 16 patients. , 1996, Journal of the American Academy of Dermatology.

[41]  W. Su,et al.  A subtle clue to the histopathologic diagnosis of early alpha 1-antitrypsin deficiency panniculitis. , 1994, Journal of the American Academy of Dermatology.

[42]  R. Winkelmann,et al.  Pseudosclerodermatous panniculitis after irradiation: an unusual complication of megavoltage treatment of breast carcinoma. , 1993, Mayo Clinic proceedings.

[43]  Philip R. Cohen,et al.  Concurrent Sweet's syndrome and erythema nodosum: a report, world literature review and mechanism of pathogenesis. , 1992, The Journal of rheumatology.

[44]  A. Hishida,et al.  Crystal-storing histiocytosis and crystalline tissue deposition in multiple myeloma. , 1991, Archives of pathology & laboratory medicine.

[45]  A. Solomon,et al.  Alpha 1-antitrypsin deficiency associated with panniculitis. , 1988, Journal of the American Academy of Dermatology.

[46]  P. Leboit,et al.  Gout presenting as lobular panniculitis. , 1987, The American Journal of dermatopathology.