Malignant atrophic papulosis (MAP) is a rare, obliterating vasculopathy affecting multiple systems, frequently with a poor prognosis. Although cutaneous lesions are often the initial presentation, systemic involvement is also common, usually with a fatal outcome. Involvement of the genitalia is very rare. We describe a 45-year-old male patient with multisytemic manifestation of MAP accompanied by painful penile ulceration. The pathogenesis of MAP is not yet fully understood and effective treatment choices are limited. In our case, the combination of pentoxifylline and dipyridamole failed to provide a beneficial effect on the progression of the disease and the patient died due to intestinal and intrathoracic manifestation of MAP. In the pres...
Bowenoid papulosis (BP), a rare disease with malignant potential, is a distinct clinicopathological ...
Abstract Waldenstrom’s macroglobulinemia is considered a lymphoma by the World Health Organization. ...
We describe the case of a 73-year-old man who presented with a 10-month history of an ulcerating les...
Malignant atrophic papulosis (MAP) is a rare, obliterating vasculopathy affecting multiple systems, ...
Abstract Malignant atrophic papulosisis is a rare, multisystem obliterative vasculopathy of unknown ...
Abstract Introduction Penile cancer is uncommon. When penile cancer is left untreated, at an advance...
Calcific uremic arteriolopathy (CUA) or calciphylaxis is a syndrome characterized by calcification o...
Chancroid is a rare infection in the United States and many other developed countries. Infrequently ...
Degos' disease, otherwise known as "malignant atrophic papulosis," is a rare condition characterized...
Malignant atrophic papulosis is a systemic vaso-occlusive disorder characterized by typical skin les...
Mycobacterium tuberculosis (TB) infection of the penis is a rare but serious problem. We report a ca...
Atrophic papulosis (Kohlmeier\u2013Degos disease or Degos disease) is a rare occlusive arteriopathy ...
Mycobacterium tuberculosis (TB) infection of the penis is a rare but serious problem. We report a ca...
OBJECTIVE To report on the largest series to date of ulceration of the external genitalia, related t...
We report a 38-year-old woman with lymphomatoid papulosis (LyP) who had nodular and papulovesicular ...
Bowenoid papulosis (BP), a rare disease with malignant potential, is a distinct clinicopathological ...
Abstract Waldenstrom’s macroglobulinemia is considered a lymphoma by the World Health Organization. ...
We describe the case of a 73-year-old man who presented with a 10-month history of an ulcerating les...
Malignant atrophic papulosis (MAP) is a rare, obliterating vasculopathy affecting multiple systems, ...
Abstract Malignant atrophic papulosisis is a rare, multisystem obliterative vasculopathy of unknown ...
Abstract Introduction Penile cancer is uncommon. When penile cancer is left untreated, at an advance...
Calcific uremic arteriolopathy (CUA) or calciphylaxis is a syndrome characterized by calcification o...
Chancroid is a rare infection in the United States and many other developed countries. Infrequently ...
Degos' disease, otherwise known as "malignant atrophic papulosis," is a rare condition characterized...
Malignant atrophic papulosis is a systemic vaso-occlusive disorder characterized by typical skin les...
Mycobacterium tuberculosis (TB) infection of the penis is a rare but serious problem. We report a ca...
Atrophic papulosis (Kohlmeier\u2013Degos disease or Degos disease) is a rare occlusive arteriopathy ...
Mycobacterium tuberculosis (TB) infection of the penis is a rare but serious problem. We report a ca...
OBJECTIVE To report on the largest series to date of ulceration of the external genitalia, related t...
We report a 38-year-old woman with lymphomatoid papulosis (LyP) who had nodular and papulovesicular ...
Bowenoid papulosis (BP), a rare disease with malignant potential, is a distinct clinicopathological ...
Abstract Waldenstrom’s macroglobulinemia is considered a lymphoma by the World Health Organization. ...
We describe the case of a 73-year-old man who presented with a 10-month history of an ulcerating les...